Canonical Allele Identifier: CA136802

Gene: VCL

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74074780C>T , CM000672.2:g.74074780C>T	GRCh38
NC_000010.10:g.75834538C>T , CM000672.1:g.75834538C>T	GRCh37
NC_000010.9:g.75504544C>T	NCBI36
NG_008868.1:g.81667C>T , LRG_383:g.81667C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.660C>T MANE Select	ENSP00000211998.5:p.Asn220=
ENST00000211998.8:c.660C>T	ENSP00000211998.4:p.Asn220=
ENST00000372755.7:c.660C>T	ENSP00000361841.3:p.Asn220=
ENST00000478896.2:n.332-26274C>T
ENST00000623461.3:n.618C>T
ENST00000624354.3:c.*415C>T	ENSP00000485551.1:n.*415C>T
NM_003373.3:c.660C>T	NP_003364.1:p.Asn220=
NM_014000.2:c.660C>T , LRG_383t1:c.660C>T	NP_054706.1:p.Asn220=
XM_005270142.1:c.660C>T	XP_005270199.1:p.Asn220=
XM_005270143.1:c.660C>T	XP_005270200.1:p.Asn220=
NM_003373.4:c.660C>T	NP_003364.1:p.Asn220=
NM_014000.3:c.660C>T MANE Select	NP_054706.1:p.Asn220=