Canonical Allele Identifier: CA915950925

Gene: DMD

Linked Data

• ClinVar Variation Id: 803857
• ClinVar RCV Id: RCV000990642
• dbSNP Id: rs1603631241

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32343184dup , CM000685.2:g.32343184dup	GRCh38
NC_000023.10:g.32361301dup , CM000685.1:g.32361301dup	GRCh37
NC_000023.9:g.32271222dup	NCBI36
NG_012232.1:g.1001426dup , LRG_199:g.1001426dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.535dup	ENSP00000350765.3:p.Glu179GlyfsTer9
ENST00000357033.9:c.5689dup MANE Select	ENSP00000354923.3:p.Glu1897GlyfsTer9
ENST00000619831.5:c.1657dup	ENSP00000479270.2:p.Glu553GlyfsTer9
ENST00000357033.8:c.5689dup	ENSP00000354923.3:p.Glu1897GlyfsTer9
ENST00000378677.6:c.5677dup	ENSP00000367948.2:p.Glu1893GlyfsTer9
ENST00000488902.5:n.336-126121dup
ENST00000493412.1:c.346dup	ENSP00000417725.1:p.Glu116GlyfsTer9
ENST00000619831.4:c.5677dup	ENSP00000479270.1:p.Glu1893GlyfsTer9
ENST00000620040.4:c.5689dup	ENSP00000478150.1:p.Glu1897GlyfsTer9
NM_000109.3:c.5665dup	NP_000100.2:p.Glu1889GlyfsTer9
NM_004006.2:c.5689dup , LRG_199t1:c.5689dup	NP_003997.1:p.Glu1897GlyfsTer9
NM_004009.3:c.5677dup	NP_004000.1:p.Glu1893GlyfsTer9
NM_004010.3:c.5320dup	NP_004001.1:p.Glu1774GlyfsTer9
NM_004011.3:c.1666dup	NP_004002.2:p.Glu556GlyfsTer9
NM_004012.3:c.1657dup	NP_004003.1:p.Glu553GlyfsTer9
XM_006724468.2:c.5689dup	XP_006724531.1:p.Glu1897GlyfsTer9
XM_006724469.2:c.5665dup	XP_006724532.1:p.Glu1889GlyfsTer9
XM_006724470.2:c.5689dup	XP_006724533.1:p.Glu1897GlyfsTer9
XM_006724471.2:c.5689dup	XP_006724534.1:p.Glu1897GlyfsTer9
XM_006724472.2:c.5560dup	XP_006724535.1:p.Glu1854GlyfsTer9
XM_006724473.2:c.5551dup	XP_006724536.1:p.Glu1851GlyfsTer9
XM_006724474.2:c.5689dup	XP_006724537.1:p.Glu1897GlyfsTer9
XM_006724475.2:c.5689dup	XP_006724538.1:p.Glu1897GlyfsTer9
XM_011545467.1:c.5566dup	XP_011543769.1:p.Glu1856GlyfsTer9
XM_011545468.1:c.5689dup	XP_011543770.1:p.Glu1897GlyfsTer9
XM_011545469.1:c.5689dup	XP_011543771.1:p.Glu1897GlyfsTer9
XM_006724469.3:c.5665dup	XP_006724532.1:p.Glu1889GlyfsTer9
XM_006724470.3:c.5689dup	XP_006724533.1:p.Glu1897GlyfsTer9
XM_006724474.3:c.5689dup	XP_006724537.1:p.Glu1897GlyfsTer9
XM_011545468.2:c.5689dup	XP_011543770.1:p.Glu1897GlyfsTer9
XM_017029328.1:c.5689dup	XP_016884817.1:p.Glu1897GlyfsTer9
XM_017029329.1:c.5689dup	XP_016884818.1:p.Glu1897GlyfsTer9
XM_017029330.2:c.5689dup	XP_016884819.1:p.Glu1897GlyfsTer9
NM_000109.4:c.5665dup	NP_000100.3:p.Glu1889GlyfsTer9
NM_004006.3:c.5689dup MANE Select	NP_003997.2:p.Glu1897GlyfsTer9
NM_004011.4:c.1666dup	NP_004002.3:p.Glu556GlyfsTer9
NM_004012.4:c.1657dup	NP_004003.2:p.Glu553GlyfsTer9