Canonical Allele Identifier: CA1919902960

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74089218G= , CM000672.2:g.74089218G=	GRCh38
NC_000010.10:g.75848976G= , CM000672.1:g.75848976G=	GRCh37
NC_000010.9:g.75518982G=	NCBI36
NG_008868.1:g.96105G= , LRG_383:g.96105G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000211998.10:c.1045G= MANE Select	ENSP00000211998.5:p.Ala349=
ENST00000211998.8:c.1045G=	ENSP00000211998.4:p.Ala349=
ENST00000372755.7:c.1045G=	ENSP00000361841.3:p.Ala349=
ENST00000436396.1:c.61G=	ENSP00000415489.1:p.Ala21=
ENST00000478896.2:n.332-11836G=
ENST00000623461.3:n.3848G=
ENST00000624354.3:c.*800G=	ENSP00000485551.1:n.*800G=
NM_003373.3:c.1045G=	NP_003364.1:p.Ala349=
NM_014000.2:c.1045G= , LRG_383t1:c.1045G=	NP_054706.1:p.Ala349=
XM_005270142.1:c.1048G=	XP_005270199.1:p.Ala350=
XM_005270143.1:c.1048G=	XP_005270200.1:p.Ala350=
XR_001747501.1:n.89+714C=
NM_003373.4:c.1045G=	NP_003364.1:p.Ala349=
NM_014000.3:c.1045G= MANE Select	NP_054706.1:p.Ala349=