Canonical Allele Identifier: CA412666618

Gene: DMD

Linked Data

• MyVariant Identifiers: chrX:g.32305808T>A (hg19) ; chrX:g.32287691T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32287691T>A , CM000685.2:g.32287691T>A	GRCh38
NC_000023.10:g.32305808T>A , CM000685.1:g.32305808T>A	GRCh37
NC_000023.9:g.32215729T>A	NCBI36
NG_012232.1:g.1056919A>T , LRG_199:g.1056919A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000358062.7:c.974A>T	ENSP00000350765.3:p.Asp325Val
ENST00000357033.9:c.6128A>T MANE Select	ENSP00000354923.3:p.Asp2043Val
ENST00000619831.5:c.2096A>T	ENSP00000479270.2:p.Asp699Val
ENST00000357033.8:c.6128A>T	ENSP00000354923.3:p.Asp2043Val
ENST00000378677.6:c.6116A>T	ENSP00000367948.2:p.Asp2039Val
ENST00000488902.5:n.336-70628A>T
ENST00000619831.4:c.6116A>T	ENSP00000479270.1:p.Asp2039Val
ENST00000620040.4:c.6128A>T	ENSP00000478150.1:p.Asp2043Val
NM_000109.3:c.6104A>T	NP_000100.2:p.Asp2035Val
NM_004006.2:c.6128A>T , LRG_199t1:c.6128A>T	NP_003997.1:p.Asp2043Val
NM_004009.3:c.6116A>T	NP_004000.1:p.Asp2039Val
NM_004010.3:c.5759A>T	NP_004001.1:p.Asp1920Val
NM_004011.3:c.2105A>T	NP_004002.2:p.Asp702Val
NM_004012.3:c.2096A>T	NP_004003.1:p.Asp699Val
XM_006724468.2:c.6128A>T	XP_006724531.1:p.Asp2043Val
XM_006724469.2:c.6104A>T	XP_006724532.1:p.Asp2035Val
XM_006724470.2:c.6128A>T	XP_006724533.1:p.Asp2043Val
XM_006724471.2:c.6128A>T	XP_006724534.1:p.Asp2043Val
XM_006724472.2:c.5999A>T	XP_006724535.1:p.Asp2000Val
XM_006724473.2:c.5990A>T	XP_006724536.1:p.Asp1997Val
XM_006724474.2:c.6128A>T	XP_006724537.1:p.Asp2043Val
XM_006724475.2:c.6128A>T	XP_006724538.1:p.Asp2043Val
XM_011545467.1:c.6005A>T	XP_011543769.1:p.Asp2002Val
XM_011545468.1:c.6128A>T	XP_011543770.1:p.Asp2043Val
XM_006724469.3:c.6104A>T	XP_006724532.1:p.Asp2035Val
XM_006724470.3:c.6128A>T	XP_006724533.1:p.Asp2043Val
XM_006724474.3:c.6128A>T	XP_006724537.1:p.Asp2043Val
XM_011545468.2:c.6128A>T	XP_011543770.1:p.Asp2043Val
XM_017029328.1:c.6128A>T	XP_016884817.1:p.Asp2043Val
XM_017029329.1:c.6128A>T	XP_016884818.1:p.Asp2043Val
XM_017029330.2:c.6128A>T	XP_016884819.1:p.Asp2043Val
XM_017029331.1:c.302A>T	XP_016884820.1:p.Asp101Val
NM_000109.4:c.6104A>T	NP_000100.3:p.Asp2035Val
NM_004006.3:c.6128A>T MANE Select	NP_003997.2:p.Asp2043Val
NM_004011.4:c.2105A>T	NP_004002.3:p.Asp702Val
NM_004012.4:c.2096A>T	NP_004003.2:p.Asp699Val