Canonical Allele Identifier: CA1919897658

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74082476C= , CM000672.2:g.74082476C=	GRCh38
NC_000010.10:g.75842234C= , CM000672.1:g.75842234C=	GRCh37
NC_000010.9:g.75512240C=	NCBI36
NG_008868.1:g.89363C= , LRG_383:g.89363C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.806C= MANE Select	ENSP00000211998.5:p.Ala269=
ENST00000211998.8:c.806C=	ENSP00000211998.4:p.Ala269=
ENST00000372755.7:c.806C=	ENSP00000361841.3:p.Ala269=
ENST00000478896.2:n.332-18578C=
ENST00000623461.3:n.3609C=
ENST00000624354.3:c.*561C=	ENSP00000485551.1:n.*561C=
NM_003373.3:c.806C=	NP_003364.1:p.Ala269=
NM_014000.2:c.806C= , LRG_383t1:c.806C=	NP_054706.1:p.Ala269=
XM_005270142.1:c.809C=	XP_005270199.1:p.Ala270=
XM_005270143.1:c.809C=	XP_005270200.1:p.Ala270=
XR_001747501.1:n.90-4749G=
NM_003373.4:c.806C=	NP_003364.1:p.Ala269=
NM_014000.3:c.806C= MANE Select	NP_054706.1:p.Ala269=