Canonical Allele Identifier: CA1919890017

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74071080C= , CM000672.2:g.74071080C=	GRCh38
NC_000010.10:g.75830838C= , CM000672.1:g.75830838C=	GRCh37
NC_000010.9:g.75500844C=	NCBI36
NG_008868.1:g.77967C= , LRG_383:g.77967C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.496C= MANE Select	ENSP00000211998.5:p.Pro166=
ENST00000211998.8:c.496C=	ENSP00000211998.4:p.Pro166=
ENST00000372755.7:c.496C=	ENSP00000361841.3:p.Pro166=
ENST00000478896.2:n.331+27927C=
ENST00000623461.3:n.454C=
ENST00000624354.3:c.*251C=	ENSP00000485551.1:n.*251C=
NM_003373.3:c.496C=	NP_003364.1:p.Pro166=
NM_014000.2:c.496C= , LRG_383t1:c.496C=	NP_054706.1:p.Pro166=
XM_005270142.1:c.496C=	XP_005270199.1:p.Pro166=
XM_005270143.1:c.496C=	XP_005270200.1:p.Pro166=
NM_003373.4:c.496C=	NP_003364.1:p.Pro166=
NM_014000.3:c.496C= MANE Select	NP_054706.1:p.Pro166=