Canonical Allele Identifier: CA412666543

Gene: DMD

Linked Data

• dbSNP Id: rs780018882
• gnomAD v4: X-32287681-T-A
• MyVariant Identifiers: chrX:g.32305798T>A (hg19) ; chrX:g.32287681T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32287681T>A , CM000685.2:g.32287681T>A	GRCh38
NC_000023.10:g.32305798T>A , CM000685.1:g.32305798T>A	GRCh37
NC_000023.9:g.32215719T>A	NCBI36
NG_012232.1:g.1056929A>T , LRG_199:g.1056929A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000358062.7:c.984A>T	ENSP00000350765.3:p.Gln328His
ENST00000357033.9:c.6138A>T MANE Select	ENSP00000354923.3:p.Gln2046His
ENST00000619831.5:c.2106A>T	ENSP00000479270.2:p.Gln702His
ENST00000357033.8:c.6138A>T	ENSP00000354923.3:p.Gln2046His
ENST00000378677.6:c.6126A>T	ENSP00000367948.2:p.Gln2042His
ENST00000488902.5:n.336-70618A>T
ENST00000619831.4:c.6126A>T	ENSP00000479270.1:p.Gln2042His
ENST00000620040.4:c.6138A>T	ENSP00000478150.1:p.Gln2046His
NM_000109.3:c.6114A>T	NP_000100.2:p.Gln2038His
NM_004006.2:c.6138A>T , LRG_199t1:c.6138A>T	NP_003997.1:p.Gln2046His
NM_004009.3:c.6126A>T	NP_004000.1:p.Gln2042His
NM_004010.3:c.5769A>T	NP_004001.1:p.Gln1923His
NM_004011.3:c.2115A>T	NP_004002.2:p.Gln705His
NM_004012.3:c.2106A>T	NP_004003.1:p.Gln702His
XM_006724468.2:c.6138A>T	XP_006724531.1:p.Gln2046His
XM_006724469.2:c.6114A>T	XP_006724532.1:p.Gln2038His
XM_006724470.2:c.6138A>T	XP_006724533.1:p.Gln2046His
XM_006724471.2:c.6138A>T	XP_006724534.1:p.Gln2046His
XM_006724472.2:c.6009A>T	XP_006724535.1:p.Gln2003His
XM_006724473.2:c.6000A>T	XP_006724536.1:p.Gln2000His
XM_006724474.2:c.6138A>T	XP_006724537.1:p.Gln2046His
XM_006724475.2:c.6138A>T	XP_006724538.1:p.Gln2046His
XM_011545467.1:c.6015A>T	XP_011543769.1:p.Gln2005His
XM_011545468.1:c.6138A>T	XP_011543770.1:p.Gln2046His
XM_006724469.3:c.6114A>T	XP_006724532.1:p.Gln2038His
XM_006724470.3:c.6138A>T	XP_006724533.1:p.Gln2046His
XM_006724474.3:c.6138A>T	XP_006724537.1:p.Gln2046His
XM_011545468.2:c.6138A>T	XP_011543770.1:p.Gln2046His
XM_017029328.1:c.6138A>T	XP_016884817.1:p.Gln2046His
XM_017029329.1:c.6138A>T	XP_016884818.1:p.Gln2046His
XM_017029330.2:c.6138A>T	XP_016884819.1:p.Gln2046His
XM_017029331.1:c.312A>T	XP_016884820.1:p.Gln104His
NM_000109.4:c.6114A>T	NP_000100.3:p.Gln2038His
NM_004006.3:c.6138A>T MANE Select	NP_003997.2:p.Gln2046His
NM_004011.4:c.2115A>T	NP_004002.3:p.Gln705His
NM_004012.4:c.2106A>T	NP_004003.2:p.Gln702His