Canonical Allele Identifier: CA5562772
Gene: VCL HGNC NCBI

Linked Data

dbSNP Id: rs376226543

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.74071066C>T , CM000672.2:g.74071066C>T GRCh38
NC_000010.10:g.75830824C>T , CM000672.1:g.75830824C>T GRCh37
NC_000010.9:g.75500830C>T NCBI36
NG_008868.1:g.77953C>T , LRG_383:g.77953C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000211998.10:c.482C>T MANE Select ENSP00000211998.5:p.Thr161Ile
ENST00000211998.8:c.482C>T ENSP00000211998.4:p.Thr161Ile
ENST00000372755.7:c.482C>T ENSP00000361841.3:p.Thr161Ile
ENST00000478896.2:n.331+27913C>T
ENST00000623461.3:n.440C>T
ENST00000624354.3:c.*237C>T ENSP00000485551.1:n.*237C>T
NM_003373.3:c.482C>T NP_003364.1:p.Thr161Ile
NM_014000.2:c.482C>T , LRG_383t1:c.482C>T NP_054706.1:p.Thr161Ile
XM_005270142.1:c.482C>T XP_005270199.1:p.Thr161Ile
XM_005270143.1:c.482C>T XP_005270200.1:p.Thr161Ile
NM_003373.4:c.482C>T NP_003364.1:p.Thr161Ile
NM_014000.3:c.482C>T MANE Select NP_054706.1:p.Thr161Ile