Canonical Allele Identifier: CA1919907027

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74114804C= , CM000672.2:g.74114804C=	GRCh38
NC_000010.10:g.75874562C= , CM000672.1:g.75874562C=	GRCh37
NC_000010.9:g.75544568C=	NCBI36
NG_008868.1:g.121691C= , LRG_383:g.121691C=

Transcript Alleles

HGVS	Amino-acid Change
NM_014000.3:c.3163C= MANE Select	NP_054706.1:p.Arg1055=
ENST00000211998.10:c.3163C= MANE Select	ENSP00000211998.5:p.Arg1055=
NM_003373.3:c.2959C=	NP_003364.1:p.Arg987=
NM_003373.4:c.2959C=	NP_003364.1:p.Arg987=
NM_014000.2:c.3163C= , LRG_383t1:c.3163C=	NP_054706.1:p.Arg1055=
ENST00000211998.8:c.3163C=	ENSP00000211998.4:p.Arg1055=
ENST00000372755.7:c.2959C=	ENSP00000361841.3:p.Arg987=
ENST00000436396.1:c.2179C=	ENSP00000415489.1:p.Arg727=
ENST00000623461.3:n.5762C=
ENST00000624354.3:c.*2918C=	ENSP00000485551.1:n.*2918C=
XM_005270142.1:c.3166C=	XP_005270199.1:p.Arg1056=
XM_005270143.1:c.2962C=	XP_005270200.1:p.Arg988=