Canonical Allele Identifier: CA2422368512

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31261065C= , CM000685.2:g.31261065C=	GRCh38
NC_000023.10:g.31279182C= , CM000685.1:g.31279182C=	GRCh37
NC_000023.9:g.31189103C=	NCBI36
NG_012232.1:g.2083545G= , LRG_199:g.2083545G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.4071-49G=	ENSP00000350765.3:n.4071-49G=
ENST00000680162.2:c.21-49G=	ENSP00000506634.2:n.21-49G=
ENST00000680768.2:c.21-49G=	ENSP00000506359.2:n.21-49G=
ENST00000682238.1:c.1845-49G=	ENSP00000508124.1:n.1845-49G=
ENST00000682322.1:c.21-49G=	ENSP00000507690.1:n.21-49G=
ENST00000682600.1:c.21-49G=	ENSP00000507640.1:n.21-49G=
ENST00000683509.1:n.742-49G=
ENST00000683675.1:n.324-49G=
ENST00000683709.1:n.743-49G=
ENST00000683957.1:n.2717-49G=
ENST00000684130.1:c.1845-49G=	ENSP00000508037.1:n.1845-49G=
ENST00000343523.7:c.1080-49G=	ENSP00000340057.4:n.1080-49G=
ENST00000357033.9:c.9225-49G= MANE Select	ENSP00000354923.3:n.9225-49G=
ENST00000619831.5:c.5193-49G=	ENSP00000479270.2:n.5193-49G=
ENST00000620040.5:c.1845-49G=	ENSP00000478150.2:n.1845-49G=
ENST00000679641.1:c.21-49G=	ENSP00000506135.1:n.21-49G=
ENST00000680355.1:c.21-49G=	ENSP00000506257.1:n.21-49G=
ENST00000680557.1:c.21-49G=	ENSP00000505164.1:n.21-49G=
ENST00000680768.1:c.-37-49G=	ENSP00000506359.1:n.-37-49G=
ENST00000680961.1:c.1845-49G=	ENSP00000506386.1:n.1845-49G=
ENST00000681153.1:c.21-49G=	ENSP00000505124.1:n.21-49G=
ENST00000681334.1:c.21-49G=	ENSP00000506066.1:n.21-49G=
ENST00000681646.1:n.2886-49G=
ENST00000681654.1:n.155-49G=
ENST00000681870.1:c.21-49G=	ENSP00000506709.1:n.21-49G=
ENST00000343523.6:c.1038-49G=	ENSP00000340057.3:n.1038-49G=
ENST00000357033.8:c.9225-49G=	ENSP00000354923.3:n.9225-49G=
ENST00000358062.6:c.2313-49G=	ENSP00000350765.2:n.2313-49G=
ENST00000359836.5:c.1845-49G=	ENSP00000352894.1:n.1845-49G=
ENST00000361471.8:c.21-49G=	ENSP00000354464.4:n.21-49G=
ENST00000378677.6:c.9213-49G=	ENSP00000367948.2:n.9213-49G=
ENST00000378680.6:c.21-49G=	ENSP00000367951.2:n.21-49G=
ENST00000378702.8:c.21-49G=	ENSP00000367974.4:n.21-49G=
ENST00000378707.7:c.1845-49G=	ENSP00000367979.3:n.1845-49G=
ENST00000378723.7:c.21-49G=	ENSP00000367997.3:n.21-49G=
ENST00000469142.1:n.244-49G=
ENST00000474231.5:c.1845-49G=	ENSP00000417123.1:n.1845-49G=
ENST00000541735.5:c.1845-49G=	ENSP00000444119.1:n.1845-49G=
ENST00000619831.4:c.9210-49G=	ENSP00000479270.1:n.9210-49G=
ENST00000620040.4:c.9222-49G=	ENSP00000478150.1:n.9222-49G=
NM_000109.3:c.9201-49G=	NP_000100.2:n.9201-49G=
NM_004006.2:c.9225-49G= , LRG_199t1:c.9225-49G=	NP_003997.1:n.9225-49G=
NM_004009.3:c.9213-49G=	NP_004000.1:n.9213-49G=
NM_004010.3:c.8856-49G=	NP_004001.1:n.8856-49G=
NM_004011.3:c.5202-49G=	NP_004002.2:n.5202-49G=
NM_004012.3:c.5193-49G=	NP_004003.1:n.5193-49G=
NM_004013.2:c.1845-49G=	NP_004004.1:n.1845-49G=
NM_004014.2:c.1038-49G=	NP_004005.1:n.1038-49G=
NM_004015.2:c.21-49G=	NP_004006.1:n.21-49G=
NM_004016.2:c.21-49G=	NP_004007.1:n.21-49G=
NM_004017.2:c.21-49G=	NP_004008.1:n.21-49G=
NM_004018.2:c.21-49G=	NP_004009.1:n.21-49G=
NM_004019.2:c.21-49G=	NP_004010.1:n.21-49G=
NM_004020.3:c.1845-49G=	NP_004011.2:n.1845-49G=
NM_004021.2:c.1845-49G=	NP_004012.1:n.1845-49G=
NM_004022.2:c.1845-49G=	NP_004013.1:n.1845-49G=
NM_004023.2:c.1845-49G=	NP_004014.1:n.1845-49G=
XM_006724468.2:c.9225-49G=	XP_006724531.1:n.9225-49G=
XM_006724469.2:c.9201-49G=	XP_006724532.1:n.9201-49G=
XM_006724470.2:c.9225-49G=	XP_006724533.1:n.9225-49G=
XM_006724471.2:c.9225-49G=	XP_006724534.1:n.9225-49G=
XM_006724472.2:c.9096-49G=	XP_006724535.1:n.9096-49G=
XM_006724473.2:c.9087-49G=	XP_006724536.1:n.9087-49G=
XM_006724474.2:c.9225-49G=	XP_006724537.1:n.9225-49G=
XM_006724475.2:c.9225-49G=	XP_006724538.1:n.9225-49G=
XM_011545467.1:c.9102-49G=	XP_011543769.1:n.9102-49G=
XM_011545468.1:c.9225-49G=	XP_011543770.1:n.9225-49G=
XM_006724469.3:c.9201-49G=	XP_006724532.1:n.9201-49G=
XM_006724470.3:c.9225-49G=	XP_006724533.1:n.9225-49G=
XM_006724474.3:c.9225-49G=	XP_006724537.1:n.9225-49G=
XM_011545468.2:c.9225-49G=	XP_011543770.1:n.9225-49G=
XM_017029328.1:c.9225-49G=	XP_016884817.1:n.9225-49G=
XM_017029331.1:c.3399-49G=	XP_016884820.1:n.3399-49G=
NM_000109.4:c.9201-49G=	NP_000100.3:n.9201-49G=
NM_004006.3:c.9225-49G= MANE Select	NP_003997.2:n.9225-49G=
NM_004011.4:c.5202-49G=	NP_004002.3:n.5202-49G=
NM_004012.4:c.5193-49G=	NP_004003.2:n.5193-49G=
NM_004015.3:c.21-49G=	NP_004006.1:n.21-49G=
NM_004016.3:c.21-49G=	NP_004007.1:n.21-49G=
NM_004017.3:c.21-49G=	NP_004008.1:n.21-49G=
NM_004018.3:c.21-49G=	NP_004009.1:n.21-49G=
NM_004019.3:c.21-49G=	NP_004010.1:n.21-49G=
NM_004021.3:c.1845-49G=	NP_004012.2:n.1845-49G=
NM_004023.3:c.1845-49G=	NP_004014.2:n.1845-49G=
NM_004013.3:c.1845-49G=	NP_004004.2:n.1845-49G=
NM_004014.3:c.1038-49G=	NP_004005.2:n.1038-49G=
NM_004020.4:c.1845-49G=	NP_004011.3:n.1845-49G=
NM_004022.3:c.1845-49G=	NP_004013.2:n.1845-49G=