Canonical Allele Identifier: CA273103

Gene: DMD

Linked Data

• ClinVar Variation Id: 11225
• ClinVar RCV Id: RCV000011976 ; RCV000255815
• dbSNP Id: rs128626235
• MyVariant Identifiers: chrX:g.32834682G>A (hg19) ; chrX:g.32816565G>A (hg38)
• PubMed: PMID:7951253

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32816565G>A , CM000685.2:g.32816565G>A	GRCh38
NC_000023.10:g.32834682G>A , CM000685.1:g.32834682G>A	GRCh37
NC_000023.9:g.32744603G>A	NCBI36
NG_012232.1:g.528045C>T , LRG_199:g.528045C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682071.1:c.64C>T	ENSP00000508133.1:p.Arg22Ter
ENST00000682437.1:n.757C>T
ENST00000682870.1:n.618C>T
ENST00000682899.1:n.640C>T
ENST00000682924.1:c.433C>T	ENSP00000508187.1:p.Arg145Ter
ENST00000683309.1:n.617C>T
ENST00000683658.1:n.778C>T
ENST00000683985.1:n.640C>T
ENST00000684056.1:n.617C>T
ENST00000684165.1:n.640C>T
ENST00000684237.1:c.433C>T	ENSP00000507277.1:p.Arg145Ter
ENST00000684292.1:n.640C>T
ENST00000684660.1:n.618C>T
ENST00000288447.9:c.409C>T	ENSP00000288447.4:p.Arg137Ter
ENST00000357033.9:c.433C>T MANE Select	ENSP00000354923.3:p.Arg145Ter
ENST00000288447.8:c.409C>T	ENSP00000288447.4:p.Arg137Ter
ENST00000357033.8:c.433C>T	ENSP00000354923.3:p.Arg145Ter
ENST00000378677.6:c.421C>T	ENSP00000367948.2:p.Arg141Ter
ENST00000420596.5:c.93+203574C>T	ENSP00000399897.1:n.93+203574C>T
ENST00000447523.1:c.246+6730C>T	ENSP00000395904.1:n.246+6730C>T
ENST00000448370.5:c.93+203574C>T	ENSP00000388559.1:n.93+203574C>T
ENST00000488902.5:n.335+203574C>T
ENST00000619831.4:c.421C>T	ENSP00000479270.1:p.Arg141Ter
ENST00000620040.4:c.433C>T	ENSP00000478150.1:p.Arg145Ter
NM_000109.3:c.409C>T	NP_000100.2:p.Arg137Ter
NM_004006.2:c.433C>T , LRG_199t1:c.433C>T	NP_003997.1:p.Arg145Ter
NM_004009.3:c.421C>T	NP_004000.1:p.Arg141Ter
NM_004010.3:c.64C>T	NP_004001.1:p.Arg22Ter
XM_006724468.2:c.433C>T	XP_006724531.1:p.Arg145Ter
XM_006724469.2:c.409C>T	XP_006724532.1:p.Arg137Ter
XM_006724470.2:c.433C>T	XP_006724533.1:p.Arg145Ter
XM_006724471.2:c.433C>T	XP_006724534.1:p.Arg145Ter
XM_006724472.2:c.433C>T	XP_006724535.1:p.Arg145Ter
XM_006724473.2:c.433C>T	XP_006724536.1:p.Arg145Ter
XM_006724474.2:c.433C>T	XP_006724537.1:p.Arg145Ter
XM_006724475.2:c.433C>T	XP_006724538.1:p.Arg145Ter
XM_011545467.1:c.433C>T	XP_011543769.1:p.Arg145Ter
XM_011545468.1:c.433C>T	XP_011543770.1:p.Arg145Ter
XM_011545469.1:c.433C>T	XP_011543771.1:p.Arg145Ter
XM_006724469.3:c.409C>T	XP_006724532.1:p.Arg137Ter
XM_006724470.3:c.433C>T	XP_006724533.1:p.Arg145Ter
XM_006724474.3:c.433C>T	XP_006724537.1:p.Arg145Ter
XM_011545468.2:c.433C>T	XP_011543770.1:p.Arg145Ter
XM_017029328.1:c.433C>T	XP_016884817.1:p.Arg145Ter
XM_017029329.1:c.433C>T	XP_016884818.1:p.Arg145Ter
XM_017029330.2:c.433C>T	XP_016884819.1:p.Arg145Ter
NM_000109.4:c.409C>T	NP_000100.3:p.Arg137Ter
NM_004006.3:c.433C>T MANE Select	NP_003997.2:p.Arg145Ter