Canonical Allele Identifier: CA1919897631

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74082459T= , CM000672.2:g.74082459T=	GRCh38
NC_000010.10:g.75842217T= , CM000672.1:g.75842217T=	GRCh37
NC_000010.9:g.75512223T=	NCBI36
NG_008868.1:g.89346T= , LRG_383:g.89346T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.789T= MANE Select	ENSP00000211998.5:p.Thr263=
ENST00000211998.8:c.789T=	ENSP00000211998.4:p.Thr263=
ENST00000372755.7:c.789T=	ENSP00000361841.3:p.Thr263=
ENST00000478896.2:n.332-18595T=
ENST00000623461.3:n.3592T=
ENST00000624354.3:c.*544T=	ENSP00000485551.1:n.*544T=
NM_003373.3:c.789T=	NP_003364.1:p.Thr263=
NM_014000.2:c.789T= , LRG_383t1:c.789T=	NP_054706.1:p.Thr263=
XM_005270142.1:c.792T=	XP_005270199.1:p.Thr264=
XM_005270143.1:c.792T=	XP_005270200.1:p.Thr264=
XR_001747501.1:n.90-4732A=
NM_003373.4:c.789T=	NP_003364.1:p.Thr263=
NM_014000.3:c.789T= MANE Select	NP_054706.1:p.Thr263=