Canonical Allele Identifier: CA290637

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32485077T= , CM000685.2:g.32485077T=	GRCh38
NC_000023.10:g.32503194T= , CM000685.1:g.32503194T=	GRCh37
NC_000023.9:g.32413115T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682899.1:n.2852A=
ENST00000683985.1:n.2852A=
ENST00000357033.9:c.2645A= MANE Select	ENSP00000354923.3:p.Asp882=
ENST00000357033.8:c.2645A=	ENSP00000354923.3:p.Asp882=
ENST00000378677.6:c.2633A=	ENSP00000367948.2:p.Asp878=
ENST00000420596.5:c.94-119878A=	ENSP00000399897.1:n.94-119878A=
ENST00000448370.5:c.94-120367A=	ENSP00000388559.1:n.94-120367A=
ENST00000488902.5:n.336-268014A=
ENST00000619831.4:c.2633A=	ENSP00000479270.1:p.Asp878=
ENST00000620040.4:c.2645A=	ENSP00000478150.1:p.Asp882=
XM_006724468.2:c.2645A=	XP_006724531.1:p.Asp882=
XM_006724469.2:c.2621A=	XP_006724532.1:p.Asp874=
XM_006724470.2:c.2645A=	XP_006724533.1:p.Asp882=
XM_006724471.2:c.2645A=	XP_006724534.1:p.Asp882=
XM_006724472.2:c.2516A=	XP_006724535.1:p.Asp839=
XM_006724473.2:c.2645A=	XP_006724536.1:p.Asp882=
XM_006724474.2:c.2645A=	XP_006724537.1:p.Asp882=
XM_006724475.2:c.2645A=	XP_006724538.1:p.Asp882=
XM_011545467.1:c.2645A=	XP_011543769.1:p.Asp882=
XM_011545468.1:c.2645A=	XP_011543770.1:p.Asp882=
XM_011545469.1:c.2645A=	XP_011543771.1:p.Asp882=
XM_006724469.3:c.2621A=	XP_006724532.1:p.Asp874=
XM_006724470.3:c.2645A=	XP_006724533.1:p.Asp882=
XM_006724474.3:c.2645A=	XP_006724537.1:p.Asp882=
XM_011545468.2:c.2645A=	XP_011543770.1:p.Asp882=
XM_017029328.1:c.2645A=	XP_016884817.1:p.Asp882=
XM_017029329.1:c.2645A=	XP_016884818.1:p.Asp882=
XM_017029330.2:c.2645A=	XP_016884819.1:p.Asp882=
NM_000109.4:c.2621A=	NP_000100.3:p.Asp874=
NM_004006.3:c.2645A= MANE Select	NP_003997.2:p.Asp882=