Canonical Allele Identifier: CA10379327

Gene: DMD

Linked Data

• ClinVar Variation Id: 1563283
• ClinVar RCV Id: RCV002206994
• dbSNP Id: rs769402316
• ExAC: X:32482748 G / T
• gnomAD v2: X-32482748-G-T
• gnomAD v3: X-32464631-G-T
• gnomAD v4: X-32464631-G-T
• MyVariant Identifiers: chrX:g.32482748G>T (hg19) ; chrX:g.32464631G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32464631G>T , CM000685.2:g.32464631G>T	GRCh38
NC_000023.10:g.32482748G>T , CM000685.1:g.32482748G>T	GRCh37
NC_000023.9:g.32392669G>T	NCBI36
NG_012232.1:g.879979C>A , LRG_199:g.879979C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682899.1:n.3438C>A
ENST00000357033.9:c.3231C>A MANE Select	ENSP00000354923.3:p.Ala1077=
ENST00000357033.8:c.3231C>A	ENSP00000354923.3:p.Ala1077=
ENST00000378677.6:c.3219C>A	ENSP00000367948.2:p.Ala1073=
ENST00000420596.5:c.94-99432C>A	ENSP00000399897.1:n.94-99432C>A
ENST00000448370.5:c.94-99921C>A	ENSP00000388559.1:n.94-99921C>A
ENST00000488902.5:n.336-247568C>A
ENST00000619831.4:c.3219C>A	ENSP00000479270.1:p.Ala1073=
ENST00000620040.4:c.3231C>A	ENSP00000478150.1:p.Ala1077=
NM_000109.3:c.3207C>A	NP_000100.2:p.Ala1069=
NM_004006.2:c.3231C>A , LRG_199t1:c.3231C>A	NP_003997.1:p.Ala1077=
NM_004009.3:c.3219C>A	NP_004000.1:p.Ala1073=
NM_004010.3:c.2862C>A	NP_004001.1:p.Ala954=
XM_006724468.2:c.3231C>A	XP_006724531.1:p.Ala1077=
XM_006724469.2:c.3207C>A	XP_006724532.1:p.Ala1069=
XM_006724470.2:c.3231C>A	XP_006724533.1:p.Ala1077=
XM_006724471.2:c.3231C>A	XP_006724534.1:p.Ala1077=
XM_006724472.2:c.3102C>A	XP_006724535.1:p.Ala1034=
XM_006724473.2:c.3231C>A	XP_006724536.1:p.Ala1077=
XM_006724474.2:c.3231C>A	XP_006724537.1:p.Ala1077=
XM_006724475.2:c.3231C>A	XP_006724538.1:p.Ala1077=
XM_011545467.1:c.3231C>A	XP_011543769.1:p.Ala1077=
XM_011545468.1:c.3231C>A	XP_011543770.1:p.Ala1077=
XM_011545469.1:c.3231C>A	XP_011543771.1:p.Ala1077=
XM_006724469.3:c.3207C>A	XP_006724532.1:p.Ala1069=
XM_006724470.3:c.3231C>A	XP_006724533.1:p.Ala1077=
XM_006724474.3:c.3231C>A	XP_006724537.1:p.Ala1077=
XM_011545468.2:c.3231C>A	XP_011543770.1:p.Ala1077=
XM_017029328.1:c.3231C>A	XP_016884817.1:p.Ala1077=
XM_017029329.1:c.3231C>A	XP_016884818.1:p.Ala1077=
XM_017029330.2:c.3231C>A	XP_016884819.1:p.Ala1077=
NM_000109.4:c.3207C>A	NP_000100.3:p.Ala1069=
NM_004006.3:c.3231C>A MANE Select	NP_003997.2:p.Ala1077=