Canonical Allele Identifier: CA255776

Gene: DMD

Linked Data

• ClinVar Variation Id: 11283
• ClinVar RCV Id: RCV000012034 ; RCV000201024 ; RCV000183404 ; RCV003323357
• dbSNP Id: rs5030730
• COSMIC: COSM1467594 ; COSM1467595 ; COSM1467596
• MyVariant Identifiers: chrX:g.32456489G>A (hg19) ; chrX:g.32438372G>A (hg38)
• PubMed: PMID:11039581 ; PMID:17041906

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32438372G>A , CM000685.2:g.32438372G>A	GRCh38
NC_000023.10:g.32456489G>A , CM000685.1:g.32456489G>A	GRCh37
NC_000023.9:g.32366410G>A	NCBI36
NG_012232.1:g.906238C>T , LRG_199:g.906238C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357033.9:c.3940C>T MANE Select	ENSP00000354923.3:p.Arg1314Ter
ENST00000357033.8:c.3940C>T	ENSP00000354923.3:p.Arg1314Ter
ENST00000378677.6:c.3928C>T	ENSP00000367948.2:p.Arg1310Ter
ENST00000420596.5:c.94-73173C>T	ENSP00000399897.1:n.94-73173C>T
ENST00000448370.5:c.94-73662C>T	ENSP00000388559.1:n.94-73662C>T
ENST00000488902.5:n.336-221309C>T
ENST00000619831.4:c.3928C>T	ENSP00000479270.1:p.Arg1310Ter
ENST00000620040.4:c.3940C>T	ENSP00000478150.1:p.Arg1314Ter
NM_000109.3:c.3916C>T	NP_000100.2:p.Arg1306Ter
NM_004006.2:c.3940C>T , LRG_199t1:c.3940C>T	NP_003997.1:p.Arg1314Ter
NM_004009.3:c.3928C>T	NP_004000.1:p.Arg1310Ter
NM_004010.3:c.3571C>T	NP_004001.1:p.Arg1191Ter
XM_006724468.2:c.3940C>T	XP_006724531.1:p.Arg1314Ter
XM_006724469.2:c.3916C>T	XP_006724532.1:p.Arg1306Ter
XM_006724470.2:c.3940C>T	XP_006724533.1:p.Arg1314Ter
XM_006724471.2:c.3940C>T	XP_006724534.1:p.Arg1314Ter
XM_006724472.2:c.3811C>T	XP_006724535.1:p.Arg1271Ter
XM_006724473.2:c.3940C>T	XP_006724536.1:p.Arg1314Ter
XM_006724474.2:c.3940C>T	XP_006724537.1:p.Arg1314Ter
XM_006724475.2:c.3940C>T	XP_006724538.1:p.Arg1314Ter
XM_011545467.1:c.3940C>T	XP_011543769.1:p.Arg1314Ter
XM_011545468.1:c.3940C>T	XP_011543770.1:p.Arg1314Ter
XM_011545469.1:c.3940C>T	XP_011543771.1:p.Arg1314Ter
XM_006724469.3:c.3916C>T	XP_006724532.1:p.Arg1306Ter
XM_006724470.3:c.3940C>T	XP_006724533.1:p.Arg1314Ter
XM_006724474.3:c.3940C>T	XP_006724537.1:p.Arg1314Ter
XM_011545468.2:c.3940C>T	XP_011543770.1:p.Arg1314Ter
XM_017029328.1:c.3940C>T	XP_016884817.1:p.Arg1314Ter
XM_017029329.1:c.3940C>T	XP_016884818.1:p.Arg1314Ter
XM_017029330.2:c.3940C>T	XP_016884819.1:p.Arg1314Ter
NM_000109.4:c.3916C>T	NP_000100.3:p.Arg1306Ter
NM_004006.3:c.3940C>T MANE Select	NP_003997.2:p.Arg1314Ter