Canonical Allele Identifier: CA2422736431

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32287615_32287616delinsAG , CM000685.2:g.32287615_32287616delinsAG	GRCh38
NC_000023.10:g.32305732_32305733delinsAG , CM000685.1:g.32305732_32305733delinsAG	GRCh37
NC_000023.9:g.32215653_32215654delinsAG	NCBI36
NG_012232.1:g.1056994_1056995delinsCT , LRG_199:g.1056994_1056995delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.1049_1050delinsCT	ENSP00000350765.3:p.Pro350=
ENST00000357033.9:c.6203_6204delinsCT MANE Select	ENSP00000354923.3:p.Pro2068=
ENST00000619831.5:c.2171_2172delinsCT	ENSP00000479270.2:p.Pro724=
ENST00000357033.8:c.6203_6204delinsCT	ENSP00000354923.3:p.Pro2068=
ENST00000378677.6:c.6191_6192delinsCT	ENSP00000367948.2:p.Pro2064=
ENST00000488902.5:n.336-70553_336-70552delinsCT
ENST00000619831.4:c.6191_6192delinsCT	ENSP00000479270.1:p.Pro2064=
ENST00000620040.4:c.6203_6204delinsCT	ENSP00000478150.1:p.Pro2068=
NM_000109.3:c.6179_6180delinsCT	NP_000100.2:p.Pro2060=
NM_004006.2:c.6203_6204delinsCT , LRG_199t1:c.6203_6204delinsCT	NP_003997.1:p.Pro2068=
NM_004009.3:c.6191_6192delinsCT	NP_004000.1:p.Pro2064=
NM_004010.3:c.5834_5835delinsCT	NP_004001.1:p.Pro1945=
NM_004011.3:c.2180_2181delinsCT	NP_004002.2:p.Pro727=
NM_004012.3:c.2171_2172delinsCT	NP_004003.1:p.Pro724=
XM_006724468.2:c.6203_6204delinsCT	XP_006724531.1:p.Pro2068=
XM_006724469.2:c.6179_6180delinsCT	XP_006724532.1:p.Pro2060=
XM_006724470.2:c.6203_6204delinsCT	XP_006724533.1:p.Pro2068=
XM_006724471.2:c.6203_6204delinsCT	XP_006724534.1:p.Pro2068=
XM_006724472.2:c.6074_6075delinsCT	XP_006724535.1:p.Pro2025=
XM_006724473.2:c.6065_6066delinsCT	XP_006724536.1:p.Pro2022=
XM_006724474.2:c.6203_6204delinsCT	XP_006724537.1:p.Pro2068=
XM_006724475.2:c.6203_6204delinsCT	XP_006724538.1:p.Pro2068=
XM_011545467.1:c.6080_6081delinsCT	XP_011543769.1:p.Pro2027=
XM_011545468.1:c.6203_6204delinsCT	XP_011543770.1:p.Pro2068=
XM_006724469.3:c.6179_6180delinsCT	XP_006724532.1:p.Pro2060=
XM_006724470.3:c.6203_6204delinsCT	XP_006724533.1:p.Pro2068=
XM_006724474.3:c.6203_6204delinsCT	XP_006724537.1:p.Pro2068=
XM_011545468.2:c.6203_6204delinsCT	XP_011543770.1:p.Pro2068=
XM_017029328.1:c.6203_6204delinsCT	XP_016884817.1:p.Pro2068=
XM_017029329.1:c.6203_6204delinsCT	XP_016884818.1:p.Pro2068=
XM_017029330.2:c.6203_6204delinsCT	XP_016884819.1:p.Pro2068=
XM_017029331.1:c.377_378delinsCT	XP_016884820.1:p.Pro126=
NM_000109.4:c.6179_6180delinsCT	NP_000100.3:p.Pro2060=
NM_004006.3:c.6203_6204delinsCT MANE Select	NP_003997.2:p.Pro2068=
NM_004011.4:c.2180_2181delinsCT	NP_004002.3:p.Pro727=
NM_004012.4:c.2171_2172delinsCT	NP_004003.2:p.Pro724=