Canonical Allele Identifier: CA1919898914

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74107254C= , CM000672.2:g.74107254C=	GRCh38
NC_000010.10:g.75867012C= , CM000672.1:g.75867012C=	GRCh37
NC_000010.9:g.75537018C=	NCBI36
NG_008868.1:g.114141C= , LRG_383:g.114141C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.2459C= MANE Select	ENSP00000211998.5:p.Ser820=
ENST00000211998.8:c.2459C=	ENSP00000211998.4:p.Ser820=
ENST00000372755.7:c.2459C=	ENSP00000361841.3:p.Ser820=
ENST00000436396.1:c.1475C=	ENSP00000415489.1:p.Ser492=
ENST00000472585.1:n.451C=
ENST00000623461.3:n.5262C=
ENST00000624354.3:c.*2214C=	ENSP00000485551.1:n.*2214C=
NM_003373.3:c.2459C=	NP_003364.1:p.Ser820=
NM_014000.2:c.2459C= , LRG_383t1:c.2459C=	NP_054706.1:p.Ser820=
XM_005270142.1:c.2462C=	XP_005270199.1:p.Ser821=
XM_005270143.1:c.2462C=	XP_005270200.1:p.Ser821=
NM_003373.4:c.2459C=	NP_003364.1:p.Ser820=
NM_014000.3:c.2459C= MANE Select	NP_054706.1:p.Ser820=