Canonical Allele Identifier: CA515715317

Gene: DMD

Linked Data

• ClinVar Variation Id: 2710116
• ClinVar RCV Id: RCV003513046
• COSMIC: COSM4977749 ; COSM4977750 ; COSM4977751
• MyVariant Identifiers: chrX:g.32472905A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32454788A>T , CM000685.2:g.32454788A>T	GRCh38
NC_000023.10:g.32472905A>T , CM000685.1:g.32472905A>T	GRCh37
NC_000023.9:g.32382826A>T	NCBI36
NG_012232.1:g.889822T>A , LRG_199:g.889822T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682899.1:n.3684T>A
ENST00000357033.9:c.3477T>A MANE Select	ENSP00000354923.3:p.Thr1159=
ENST00000357033.8:c.3477T>A	ENSP00000354923.3:p.Thr1159=
ENST00000378677.6:c.3465T>A	ENSP00000367948.2:p.Thr1155=
ENST00000420596.5:c.94-89589T>A	ENSP00000399897.1:n.94-89589T>A
ENST00000448370.5:c.94-90078T>A	ENSP00000388559.1:n.94-90078T>A
ENST00000488902.5:n.336-237725T>A
ENST00000619831.4:c.3465T>A	ENSP00000479270.1:p.Thr1155=
ENST00000620040.4:c.3477T>A	ENSP00000478150.1:p.Thr1159=
NM_000109.3:c.3453T>A	NP_000100.2:p.Thr1151=
NM_004006.2:c.3477T>A , LRG_199t1:c.3477T>A	NP_003997.1:p.Thr1159=
NM_004009.3:c.3465T>A	NP_004000.1:p.Thr1155=
NM_004010.3:c.3108T>A	NP_004001.1:p.Thr1036=
XM_006724468.2:c.3477T>A	XP_006724531.1:p.Thr1159=
XM_006724469.2:c.3453T>A	XP_006724532.1:p.Thr1151=
XM_006724470.2:c.3477T>A	XP_006724533.1:p.Thr1159=
XM_006724471.2:c.3477T>A	XP_006724534.1:p.Thr1159=
XM_006724472.2:c.3348T>A	XP_006724535.1:p.Thr1116=
XM_006724473.2:c.3477T>A	XP_006724536.1:p.Thr1159=
XM_006724474.2:c.3477T>A	XP_006724537.1:p.Thr1159=
XM_006724475.2:c.3477T>A	XP_006724538.1:p.Thr1159=
XM_011545467.1:c.3477T>A	XP_011543769.1:p.Thr1159=
XM_011545468.1:c.3477T>A	XP_011543770.1:p.Thr1159=
XM_011545469.1:c.3477T>A	XP_011543771.1:p.Thr1159=
XM_006724469.3:c.3453T>A	XP_006724532.1:p.Thr1151=
XM_006724470.3:c.3477T>A	XP_006724533.1:p.Thr1159=
XM_006724474.3:c.3477T>A	XP_006724537.1:p.Thr1159=
XM_011545468.2:c.3477T>A	XP_011543770.1:p.Thr1159=
XM_017029328.1:c.3477T>A	XP_016884817.1:p.Thr1159=
XM_017029329.1:c.3477T>A	XP_016884818.1:p.Thr1159=
XM_017029330.2:c.3477T>A	XP_016884819.1:p.Thr1159=
NM_000109.4:c.3453T>A	NP_000100.3:p.Thr1151=
NM_004006.3:c.3477T>A MANE Select	NP_003997.2:p.Thr1159=