Canonical Allele Identifier: CA515713997

Gene: DMD

Linked Data

• MyVariant Identifiers: chrX:g.32361332A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32343215A>T , CM000685.2:g.32343215A>T	GRCh38
NC_000023.10:g.32361332A>T , CM000685.1:g.32361332A>T	GRCh37
NC_000023.9:g.32271253A>T	NCBI36
NG_012232.1:g.1001395T>A , LRG_199:g.1001395T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.504T>A	ENSP00000350765.3:p.Ala168=
ENST00000357033.9:c.5658T>A MANE Select	ENSP00000354923.3:p.Ala1886=
ENST00000619831.5:c.1626T>A	ENSP00000479270.2:p.Ala542=
ENST00000357033.8:c.5658T>A	ENSP00000354923.3:p.Ala1886=
ENST00000378677.6:c.5646T>A	ENSP00000367948.2:p.Ala1882=
ENST00000488902.5:n.336-126152T>A
ENST00000493412.1:c.315T>A	ENSP00000417725.1:p.Ala105=
ENST00000619831.4:c.5646T>A	ENSP00000479270.1:p.Ala1882=
ENST00000620040.4:c.5658T>A	ENSP00000478150.1:p.Ala1886=
NM_000109.3:c.5634T>A	NP_000100.2:p.Ala1878=
NM_004006.2:c.5658T>A , LRG_199t1:c.5658T>A	NP_003997.1:p.Ala1886=
NM_004009.3:c.5646T>A	NP_004000.1:p.Ala1882=
NM_004010.3:c.5289T>A	NP_004001.1:p.Ala1763=
NM_004011.3:c.1635T>A	NP_004002.2:p.Ala545=
NM_004012.3:c.1626T>A	NP_004003.1:p.Ala542=
XM_006724468.2:c.5658T>A	XP_006724531.1:p.Ala1886=
XM_006724469.2:c.5634T>A	XP_006724532.1:p.Ala1878=
XM_006724470.2:c.5658T>A	XP_006724533.1:p.Ala1886=
XM_006724471.2:c.5658T>A	XP_006724534.1:p.Ala1886=
XM_006724472.2:c.5529T>A	XP_006724535.1:p.Ala1843=
XM_006724473.2:c.5520T>A	XP_006724536.1:p.Ala1840=
XM_006724474.2:c.5658T>A	XP_006724537.1:p.Ala1886=
XM_006724475.2:c.5658T>A	XP_006724538.1:p.Ala1886=
XM_011545467.1:c.5535T>A	XP_011543769.1:p.Ala1845=
XM_011545468.1:c.5658T>A	XP_011543770.1:p.Ala1886=
XM_011545469.1:c.5658T>A	XP_011543771.1:p.Ala1886=
XM_006724469.3:c.5634T>A	XP_006724532.1:p.Ala1878=
XM_006724470.3:c.5658T>A	XP_006724533.1:p.Ala1886=
XM_006724474.3:c.5658T>A	XP_006724537.1:p.Ala1886=
XM_011545468.2:c.5658T>A	XP_011543770.1:p.Ala1886=
XM_017029328.1:c.5658T>A	XP_016884817.1:p.Ala1886=
XM_017029329.1:c.5658T>A	XP_016884818.1:p.Ala1886=
XM_017029330.2:c.5658T>A	XP_016884819.1:p.Ala1886=
NM_000109.4:c.5634T>A	NP_000100.3:p.Ala1878=
NM_004006.3:c.5658T>A MANE Select	NP_003997.2:p.Ala1886=
NM_004011.4:c.1635T>A	NP_004002.3:p.Ala545=
NM_004012.4:c.1626T>A	NP_004003.2:p.Ala542=