Canonical Allele Identifier: CA1919890012

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74071076T= , CM000672.2:g.74071076T=	GRCh38
NC_000010.10:g.75830834T= , CM000672.1:g.75830834T=	GRCh37
NC_000010.9:g.75500840T=	NCBI36
NG_008868.1:g.77963T= , LRG_383:g.77963T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.492T= MANE Select	ENSP00000211998.5:p.Leu164=
ENST00000211998.8:c.492T=	ENSP00000211998.4:p.Leu164=
ENST00000372755.7:c.492T=	ENSP00000361841.3:p.Leu164=
ENST00000478896.2:n.331+27923T=
ENST00000623461.3:n.450T=
ENST00000624354.3:c.*247T=	ENSP00000485551.1:n.*247T=
NM_003373.3:c.492T=	NP_003364.1:p.Leu164=
NM_014000.2:c.492T= , LRG_383t1:c.492T=	NP_054706.1:p.Leu164=
XM_005270142.1:c.492T=	XP_005270199.1:p.Leu164=
XM_005270143.1:c.492T=	XP_005270200.1:p.Leu164=
NM_003373.4:c.492T=	NP_003364.1:p.Leu164=
NM_014000.3:c.492T= MANE Select	NP_054706.1:p.Leu164=