Canonical Allele Identifier: CA2573158789

Gene: DMD

Linked Data

• ClinVar Variation Id: 1369227
• ClinVar RCV Id: RCV001894847
• dbSNP Id: rs2146991715

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32343224del , CM000685.2:g.32343224del	GRCh38
NC_000023.10:g.32361341del , CM000685.1:g.32361341del	GRCh37
NC_000023.9:g.32271262del	NCBI36
NG_012232.1:g.1001386del , LRG_199:g.1001386del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.495del	ENSP00000350765.3:p.Arg166GlyfsTer7
ENST00000357033.9:c.5649del MANE Select	ENSP00000354923.3:p.Arg1884GlyfsTer7
ENST00000619831.5:c.1617del	ENSP00000479270.2:p.Arg540GlyfsTer7
ENST00000357033.8:c.5649del	ENSP00000354923.3:p.Arg1884GlyfsTer7
ENST00000378677.6:c.5637del	ENSP00000367948.2:p.Arg1880GlyfsTer7
ENST00000488902.5:n.336-126161del
ENST00000493412.1:c.306del	ENSP00000417725.1:p.Arg103GlyfsTer7
ENST00000619831.4:c.5637del	ENSP00000479270.1:p.Arg1880GlyfsTer7
ENST00000620040.4:c.5649del	ENSP00000478150.1:p.Arg1884GlyfsTer7
NM_000109.3:c.5625del	NP_000100.2:p.Arg1876GlyfsTer7
NM_004006.2:c.5649del , LRG_199t1:c.5649del	NP_003997.1:p.Arg1884GlyfsTer7
NM_004009.3:c.5637del	NP_004000.1:p.Arg1880GlyfsTer7
NM_004010.3:c.5280del	NP_004001.1:p.Arg1761GlyfsTer7
NM_004011.3:c.1626del	NP_004002.2:p.Arg543GlyfsTer7
NM_004012.3:c.1617del	NP_004003.1:p.Arg540GlyfsTer7
XM_006724468.2:c.5649del	XP_006724531.1:p.Arg1884GlyfsTer7
XM_006724469.2:c.5625del	XP_006724532.1:p.Arg1876GlyfsTer7
XM_006724470.2:c.5649del	XP_006724533.1:p.Arg1884GlyfsTer7
XM_006724471.2:c.5649del	XP_006724534.1:p.Arg1884GlyfsTer7
XM_006724472.2:c.5520del	XP_006724535.1:p.Arg1841GlyfsTer7
XM_006724473.2:c.5511del	XP_006724536.1:p.Arg1838GlyfsTer7
XM_006724474.2:c.5649del	XP_006724537.1:p.Arg1884GlyfsTer7
XM_006724475.2:c.5649del	XP_006724538.1:p.Arg1884GlyfsTer7
XM_011545467.1:c.5526del	XP_011543769.1:p.Arg1843GlyfsTer7
XM_011545468.1:c.5649del	XP_011543770.1:p.Arg1884GlyfsTer7
XM_011545469.1:c.5649del	XP_011543771.1:p.Arg1884GlyfsTer7
XM_006724469.3:c.5625del	XP_006724532.1:p.Arg1876GlyfsTer7
XM_006724470.3:c.5649del	XP_006724533.1:p.Arg1884GlyfsTer7
XM_006724474.3:c.5649del	XP_006724537.1:p.Arg1884GlyfsTer7
XM_011545468.2:c.5649del	XP_011543770.1:p.Arg1884GlyfsTer7
XM_017029328.1:c.5649del	XP_016884817.1:p.Arg1884GlyfsTer7
XM_017029329.1:c.5649del	XP_016884818.1:p.Arg1884GlyfsTer7
XM_017029330.2:c.5649del	XP_016884819.1:p.Arg1884GlyfsTer7
NM_000109.4:c.5625del	NP_000100.3:p.Arg1876GlyfsTer7
NM_004006.3:c.5649del MANE Select	NP_003997.2:p.Arg1884GlyfsTer7
NM_004011.4:c.1626del	NP_004002.3:p.Arg543GlyfsTer7
NM_004012.4:c.1617del	NP_004003.2:p.Arg540GlyfsTer7