Canonical Allele Identifier: CA1919905817

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74112067C= , CM000672.2:g.74112067C=	GRCh38
NC_000010.10:g.75871825C= , CM000672.1:g.75871825C=	GRCh37
NC_000010.9:g.75541831C=	NCBI36
NG_008868.1:g.118954C= , LRG_383:g.118954C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000211998.10:c.2904C= MANE Select	ENSP00000211998.5:p.Ala968=
ENST00000211998.8:c.2904C=	ENSP00000211998.4:p.Ala968=
ENST00000372755.7:c.2746-2117C=	ENSP00000361841.3:n.2746-2117C=
ENST00000436396.1:c.1920C=	ENSP00000415489.1:p.Ala640=
ENST00000623461.3:n.5549-2117C=
ENST00000624354.3:c.*2659C=	ENSP00000485551.1:n.*2659C=
NM_003373.3:c.2746-2117C=	NP_003364.1:n.2746-2117C=
NM_014000.2:c.2904C= , LRG_383t1:c.2904C=	NP_054706.1:p.Ala968=
XM_005270142.1:c.2907C=	XP_005270199.1:p.Ala969=
XM_005270143.1:c.2749-2117C=	XP_005270200.1:n.2749-2117C=
NM_003373.4:c.2746-2117C=	NP_003364.1:n.2746-2117C=
NM_014000.3:c.2904C= MANE Select	NP_054706.1:p.Ala968=