Canonical Allele Identifier: CA1919905773

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74111978T= , CM000672.2:g.74111978T=	GRCh38
NC_000010.10:g.75871736T= , CM000672.1:g.75871736T=	GRCh37
NC_000010.9:g.75541742T=	NCBI36
NG_008868.1:g.118865T= , LRG_383:g.118865T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.2815T= MANE Select	ENSP00000211998.5:p.Phe939=
ENST00000211998.8:c.2815T=	ENSP00000211998.4:p.Phe939=
ENST00000372755.7:c.2746-2206T=	ENSP00000361841.3:n.2746-2206T=
ENST00000436396.1:c.1831T=	ENSP00000415489.1:p.Phe611=
ENST00000623461.3:n.5549-2206T=
ENST00000624354.3:c.*2570T=	ENSP00000485551.1:n.*2570T=
NM_003373.3:c.2746-2206T=	NP_003364.1:n.2746-2206T=
NM_014000.2:c.2815T= , LRG_383t1:c.2815T=	NP_054706.1:p.Phe939=
XM_005270142.1:c.2818T=	XP_005270199.1:p.Phe940=
XM_005270143.1:c.2749-2206T=	XP_005270200.1:n.2749-2206T=
NM_003373.4:c.2746-2206T=	NP_003364.1:n.2746-2206T=
NM_014000.3:c.2815T= MANE Select	NP_054706.1:p.Phe939=