Canonical Allele Identifier: CA412666129

Gene: DMD

Linked Data

• ClinVar Variation Id: 585786
• ClinVar RCV Id: RCV000711465 ; RCV001830576 ; RCV002534496 ; RCV003165943
• dbSNP Id: rs1468473458
• gnomAD v3: X-32287623-C-A
• gnomAD v4: X-32287623-C-A
• MyVariant Identifiers: chrX:g.32305740C>A (hg19) ; chrX:g.32287623C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32287623C>A , CM000685.2:g.32287623C>A	GRCh38
NC_000023.10:g.32305740C>A , CM000685.1:g.32305740C>A	GRCh37
NC_000023.9:g.32215661C>A	NCBI36
NG_012232.1:g.1056987G>T , LRG_199:g.1056987G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.1042G>T	ENSP00000350765.3:p.Ala348Ser
ENST00000357033.9:c.6196G>T MANE Select	ENSP00000354923.3:p.Ala2066Ser
ENST00000619831.5:c.2164G>T	ENSP00000479270.2:p.Ala722Ser
ENST00000357033.8:c.6196G>T	ENSP00000354923.3:p.Ala2066Ser
ENST00000378677.6:c.6184G>T	ENSP00000367948.2:p.Ala2062Ser
ENST00000488902.5:n.336-70560G>T
ENST00000619831.4:c.6184G>T	ENSP00000479270.1:p.Ala2062Ser
ENST00000620040.4:c.6196G>T	ENSP00000478150.1:p.Ala2066Ser
NM_000109.3:c.6172G>T	NP_000100.2:p.Ala2058Ser
NM_004006.2:c.6196G>T , LRG_199t1:c.6196G>T	NP_003997.1:p.Ala2066Ser
NM_004009.3:c.6184G>T	NP_004000.1:p.Ala2062Ser
NM_004010.3:c.5827G>T	NP_004001.1:p.Ala1943Ser
NM_004011.3:c.2173G>T	NP_004002.2:p.Ala725Ser
NM_004012.3:c.2164G>T	NP_004003.1:p.Ala722Ser
XM_006724468.2:c.6196G>T	XP_006724531.1:p.Ala2066Ser
XM_006724469.2:c.6172G>T	XP_006724532.1:p.Ala2058Ser
XM_006724470.2:c.6196G>T	XP_006724533.1:p.Ala2066Ser
XM_006724471.2:c.6196G>T	XP_006724534.1:p.Ala2066Ser
XM_006724472.2:c.6067G>T	XP_006724535.1:p.Ala2023Ser
XM_006724473.2:c.6058G>T	XP_006724536.1:p.Ala2020Ser
XM_006724474.2:c.6196G>T	XP_006724537.1:p.Ala2066Ser
XM_006724475.2:c.6196G>T	XP_006724538.1:p.Ala2066Ser
XM_011545467.1:c.6073G>T	XP_011543769.1:p.Ala2025Ser
XM_011545468.1:c.6196G>T	XP_011543770.1:p.Ala2066Ser
XM_006724469.3:c.6172G>T	XP_006724532.1:p.Ala2058Ser
XM_006724470.3:c.6196G>T	XP_006724533.1:p.Ala2066Ser
XM_006724474.3:c.6196G>T	XP_006724537.1:p.Ala2066Ser
XM_011545468.2:c.6196G>T	XP_011543770.1:p.Ala2066Ser
XM_017029328.1:c.6196G>T	XP_016884817.1:p.Ala2066Ser
XM_017029329.1:c.6196G>T	XP_016884818.1:p.Ala2066Ser
XM_017029330.2:c.6196G>T	XP_016884819.1:p.Ala2066Ser
XM_017029331.1:c.370G>T	XP_016884820.1:p.Ala124Ser
NM_000109.4:c.6172G>T	NP_000100.3:p.Ala2058Ser
NM_004006.3:c.6196G>T MANE Select	NP_003997.2:p.Ala2066Ser
NM_004011.4:c.2173G>T	NP_004002.3:p.Ala725Ser
NM_004012.4:c.2164G>T	NP_004003.2:p.Ala722Ser