Canonical Allele Identifier: CA2422760774

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32343150T= , CM000685.2:g.32343150T=	GRCh38
NC_000023.10:g.32361267T= , CM000685.1:g.32361267T=	GRCh37
NC_000023.9:g.32271188T=	NCBI36
NG_012232.1:g.1001460A= , LRG_199:g.1001460A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.569A=	ENSP00000350765.3:p.Asp190=
ENST00000357033.9:c.5723A= MANE Select	ENSP00000354923.3:p.Asp1908=
ENST00000619831.5:c.1691A=	ENSP00000479270.2:p.Asp564=
ENST00000357033.8:c.5723A=	ENSP00000354923.3:p.Asp1908=
ENST00000378677.6:c.5711A=	ENSP00000367948.2:p.Asp1904=
ENST00000488902.5:n.336-126087A=
ENST00000493412.1:c.380A=	ENSP00000417725.1:p.Asp127=
ENST00000619831.4:c.5711A=	ENSP00000479270.1:p.Asp1904=
ENST00000620040.4:c.5723A=	ENSP00000478150.1:p.Asp1908=
NM_000109.3:c.5699A=	NP_000100.2:p.Asp1900=
NM_004006.2:c.5723A= , LRG_199t1:c.5723A=	NP_003997.1:p.Asp1908=
NM_004009.3:c.5711A=	NP_004000.1:p.Asp1904=
NM_004010.3:c.5354A=	NP_004001.1:p.Asp1785=
NM_004011.3:c.1700A=	NP_004002.2:p.Asp567=
NM_004012.3:c.1691A=	NP_004003.1:p.Asp564=
XM_006724468.2:c.5723A=	XP_006724531.1:p.Asp1908=
XM_006724469.2:c.5699A=	XP_006724532.1:p.Asp1900=
XM_006724470.2:c.5723A=	XP_006724533.1:p.Asp1908=
XM_006724471.2:c.5723A=	XP_006724534.1:p.Asp1908=
XM_006724472.2:c.5594A=	XP_006724535.1:p.Asp1865=
XM_006724473.2:c.5585A=	XP_006724536.1:p.Asp1862=
XM_006724474.2:c.5723A=	XP_006724537.1:p.Asp1908=
XM_006724475.2:c.5723A=	XP_006724538.1:p.Asp1908=
XM_011545467.1:c.5600A=	XP_011543769.1:p.Asp1867=
XM_011545468.1:c.5723A=	XP_011543770.1:p.Asp1908=
XM_011545469.1:c.5723A=	XP_011543771.1:p.Asp1908=
XM_006724469.3:c.5699A=	XP_006724532.1:p.Asp1900=
XM_006724470.3:c.5723A=	XP_006724533.1:p.Asp1908=
XM_006724474.3:c.5723A=	XP_006724537.1:p.Asp1908=
XM_011545468.2:c.5723A=	XP_011543770.1:p.Asp1908=
XM_017029328.1:c.5723A=	XP_016884817.1:p.Asp1908=
XM_017029329.1:c.5723A=	XP_016884818.1:p.Asp1908=
XM_017029330.2:c.5723A=	XP_016884819.1:p.Asp1908=
NM_000109.4:c.5699A=	NP_000100.3:p.Asp1900=
NM_004006.3:c.5723A= MANE Select	NP_003997.2:p.Asp1908=
NM_004011.4:c.1700A=	NP_004002.3:p.Asp567=
NM_004012.4:c.1691A=	NP_004003.2:p.Asp564=