Canonical Allele Identifier: CA1919889988

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74071056G= , CM000672.2:g.74071056G=	GRCh38
NC_000010.10:g.75830814G= , CM000672.1:g.75830814G=	GRCh37
NC_000010.9:g.75500820G=	NCBI36
NG_008868.1:g.77943G= , LRG_383:g.77943G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.472G= MANE Select	ENSP00000211998.5:p.Val158=
ENST00000211998.8:c.472G=	ENSP00000211998.4:p.Val158=
ENST00000372755.7:c.472G=	ENSP00000361841.3:p.Val158=
ENST00000478896.2:n.331+27903G=
ENST00000623461.3:n.430G=
ENST00000624354.3:c.*227G=	ENSP00000485551.1:n.*227G=
NM_003373.3:c.472G=	NP_003364.1:p.Val158=
NM_014000.2:c.472G= , LRG_383t1:c.472G=	NP_054706.1:p.Val158=
XM_005270142.1:c.472G=	XP_005270199.1:p.Val158=
XM_005270143.1:c.472G=	XP_005270200.1:p.Val158=
NM_003373.4:c.472G=	NP_003364.1:p.Val158=
NM_014000.3:c.472G= MANE Select	NP_054706.1:p.Val158=