Canonical Allele Identifier: CA1919893079

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74101003C= , CM000672.2:g.74101003C=	GRCh38
NC_000010.10:g.75860761C= , CM000672.1:g.75860761C=	GRCh37
NC_000010.9:g.75530767C=	NCBI36
NG_008868.1:g.107890C= , LRG_383:g.107890C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000211998.10:c.1928C= MANE Select	ENSP00000211998.5:p.Thr643=
ENST00000211998.8:c.1928C=	ENSP00000211998.4:p.Thr643=
ENST00000372755.7:c.1928C=	ENSP00000361841.3:p.Thr643=
ENST00000436396.1:c.944C=	ENSP00000415489.1:p.Thr315=
ENST00000478896.2:n.332-51C=
ENST00000623461.3:n.4731C=
ENST00000624354.3:c.*1683C=	ENSP00000485551.1:n.*1683C=
NM_003373.3:c.1928C=	NP_003364.1:p.Thr643=
NM_014000.2:c.1928C= , LRG_383t1:c.1928C=	NP_054706.1:p.Thr643=
XM_005270142.1:c.1931C=	XP_005270199.1:p.Thr644=
XM_005270143.1:c.1931C=	XP_005270200.1:p.Thr644=
NM_003373.4:c.1928C=	NP_003364.1:p.Thr643=
NM_014000.3:c.1928C= MANE Select	NP_054706.1:p.Thr643=