Canonical Allele Identifier: CA2422368490

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31260970_31260972delinsGCT , CM000685.2:g.31260970_31260972delinsGCT	GRCh38
NC_000023.10:g.31279087_31279089delinsGCT , CM000685.1:g.31279087_31279089delinsGCT	GRCh37
NC_000023.9:g.31189008_31189010delinsGCT	NCBI36
NG_012232.1:g.2083638_2083640delinsAGC , LRG_199:g.2083638_2083640delinsAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.4115_4117delinsAGC	ENSP00000350765.3:p.Glu1372=
ENST00000680162.2:c.65_67delinsAGC	ENSP00000506634.2:p.Glu22=
ENST00000680768.2:c.65_67delinsAGC	ENSP00000506359.2:p.Glu22=
ENST00000682238.1:c.1889_1891delinsAGC	ENSP00000508124.1:p.Glu630=
ENST00000682322.1:c.65_67delinsAGC	ENSP00000507690.1:p.Glu22=
ENST00000682600.1:c.65_67delinsAGC	ENSP00000507640.1:p.Glu22=
ENST00000683509.1:n.786_788delinsAGC
ENST00000683675.1:n.368_370delinsAGC
ENST00000683709.1:n.787_789delinsAGC
ENST00000683957.1:n.2761_2763delinsAGC
ENST00000684130.1:c.1889_1891delinsAGC	ENSP00000508037.1:p.Glu630=
ENST00000343523.7:c.1124_1126delinsAGC	ENSP00000340057.4:p.Glu375=
ENST00000357033.9:c.9269_9271delinsAGC MANE Select	ENSP00000354923.3:p.Glu3090=
ENST00000619831.5:c.5237_5239delinsAGC	ENSP00000479270.2:p.Glu1746=
ENST00000620040.5:c.1889_1891delinsAGC	ENSP00000478150.2:p.Glu630=
ENST00000679641.1:c.65_67delinsAGC	ENSP00000506135.1:p.Glu22=
ENST00000680216.1:c.45_47delinsAGC
ENST00000680355.1:c.65_67delinsAGC	ENSP00000506257.1:p.Glu22=
ENST00000680557.1:c.65_67delinsAGC	ENSP00000505164.1:p.Glu22=
ENST00000680768.1:c.8_10delinsAGC	ENSP00000506359.1:p.Glu3=
ENST00000680961.1:c.1889_1891delinsAGC	ENSP00000506386.1:p.Glu630=
ENST00000681153.1:c.65_67delinsAGC	ENSP00000505124.1:p.Glu22=
ENST00000681334.1:c.65_67delinsAGC	ENSP00000506066.1:p.Glu22=
ENST00000681646.1:n.2930_2932delinsAGC
ENST00000681654.1:n.199_201delinsAGC
ENST00000681870.1:c.65_67delinsAGC	ENSP00000506709.1:p.Glu22=
ENST00000343523.6:c.1082_1084delinsAGC	ENSP00000340057.3:p.Glu361=
ENST00000357033.8:c.9269_9271delinsAGC	ENSP00000354923.3:p.Glu3090=
ENST00000358062.6:c.2357_2359delinsAGC	ENSP00000350765.2:p.Glu786=
ENST00000359836.5:c.1889_1891delinsAGC	ENSP00000352894.1:p.Glu630=
ENST00000361471.8:c.65_67delinsAGC	ENSP00000354464.4:p.Glu22=
ENST00000378677.6:c.9257_9259delinsAGC	ENSP00000367948.2:p.Glu3086=
ENST00000378680.6:c.65_67delinsAGC	ENSP00000367951.2:p.Glu22=
ENST00000378702.8:c.65_67delinsAGC	ENSP00000367974.4:p.Glu22=
ENST00000378707.7:c.1889_1891delinsAGC	ENSP00000367979.3:p.Glu630=
ENST00000378723.7:c.65_67delinsAGC	ENSP00000367997.3:p.Glu22=
ENST00000469142.1:n.288_290delinsAGC
ENST00000474231.5:c.1889_1891delinsAGC	ENSP00000417123.1:p.Glu630=
ENST00000541735.5:c.1889_1891delinsAGC	ENSP00000444119.1:p.Glu630=
ENST00000619831.4:c.9254_9256delinsAGC	ENSP00000479270.1:p.Glu3085=
ENST00000620040.4:c.9266_9268delinsAGC	ENSP00000478150.1:p.Glu3089=
NM_000109.3:c.9245_9247delinsAGC	NP_000100.2:p.Glu3082=
NM_004006.2:c.9269_9271delinsAGC , LRG_199t1:c.9269_9271delinsAGC	NP_003997.1:p.Glu3090=
NM_004009.3:c.9257_9259delinsAGC	NP_004000.1:p.Glu3086=
NM_004010.3:c.8900_8902delinsAGC	NP_004001.1:p.Glu2967=
NM_004011.3:c.5246_5248delinsAGC	NP_004002.2:p.Glu1749=
NM_004012.3:c.5237_5239delinsAGC	NP_004003.1:p.Glu1746=
NM_004013.2:c.1889_1891delinsAGC	NP_004004.1:p.Glu630=
NM_004014.2:c.1082_1084delinsAGC	NP_004005.1:p.Glu361=
NM_004015.2:c.65_67delinsAGC	NP_004006.1:p.Glu22=
NM_004016.2:c.65_67delinsAGC	NP_004007.1:p.Glu22=
NM_004017.2:c.65_67delinsAGC	NP_004008.1:p.Glu22=
NM_004018.2:c.65_67delinsAGC	NP_004009.1:p.Glu22=
NM_004019.2:c.65_67delinsAGC	NP_004010.1:p.Glu22=
NM_004020.3:c.1889_1891delinsAGC	NP_004011.2:p.Glu630=
NM_004021.2:c.1889_1891delinsAGC	NP_004012.1:p.Glu630=
NM_004022.2:c.1889_1891delinsAGC	NP_004013.1:p.Glu630=
NM_004023.2:c.1889_1891delinsAGC	NP_004014.1:p.Glu630=
XM_006724468.2:c.9269_9271delinsAGC	XP_006724531.1:p.Glu3090=
XM_006724469.2:c.9245_9247delinsAGC	XP_006724532.1:p.Glu3082=
XM_006724470.2:c.9269_9271delinsAGC	XP_006724533.1:p.Glu3090=
XM_006724471.2:c.9269_9271delinsAGC	XP_006724534.1:p.Glu3090=
XM_006724472.2:c.9140_9142delinsAGC	XP_006724535.1:p.Glu3047=
XM_006724473.2:c.9131_9133delinsAGC	XP_006724536.1:p.Glu3044=
XM_006724474.2:c.9269_9271delinsAGC	XP_006724537.1:p.Glu3090=
XM_006724475.2:c.9269_9271delinsAGC	XP_006724538.1:p.Glu3090=
XM_011545467.1:c.9146_9148delinsAGC	XP_011543769.1:p.Glu3049=
XM_011545468.1:c.9269_9271delinsAGC	XP_011543770.1:p.Glu3090=
XM_006724469.3:c.9245_9247delinsAGC	XP_006724532.1:p.Glu3082=
XM_006724470.3:c.9269_9271delinsAGC	XP_006724533.1:p.Glu3090=
XM_006724474.3:c.9269_9271delinsAGC	XP_006724537.1:p.Glu3090=
XM_011545468.2:c.9269_9271delinsAGC	XP_011543770.1:p.Glu3090=
XM_017029328.1:c.9269_9271delinsAGC	XP_016884817.1:p.Glu3090=
XM_017029331.1:c.3443_3445delinsAGC	XP_016884820.1:p.Glu1148=
NM_000109.4:c.9245_9247delinsAGC	NP_000100.3:p.Glu3082=
NM_004006.3:c.9269_9271delinsAGC MANE Select	NP_003997.2:p.Glu3090=
NM_004011.4:c.5246_5248delinsAGC	NP_004002.3:p.Glu1749=
NM_004012.4:c.5237_5239delinsAGC	NP_004003.2:p.Glu1746=
NM_004015.3:c.65_67delinsAGC	NP_004006.1:p.Glu22=
NM_004016.3:c.65_67delinsAGC	NP_004007.1:p.Glu22=
NM_004017.3:c.65_67delinsAGC	NP_004008.1:p.Glu22=
NM_004018.3:c.65_67delinsAGC	NP_004009.1:p.Glu22=
NM_004019.3:c.65_67delinsAGC	NP_004010.1:p.Glu22=
NM_004021.3:c.1889_1891delinsAGC	NP_004012.2:p.Glu630=
NM_004023.3:c.1889_1891delinsAGC	NP_004014.2:p.Glu630=
NM_004013.3:c.1889_1891delinsAGC	NP_004004.2:p.Glu630=
NM_004014.3:c.1082_1084delinsAGC	NP_004005.2:p.Glu361=
NM_004020.4:c.1889_1891delinsAGC	NP_004011.3:p.Glu630=
NM_004022.3:c.1889_1891delinsAGC	NP_004013.2:p.Glu630=