Canonical Allele Identifier: CA377266761
Gene: VCL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.74071064C>G , CM000672.2:g.74071064C>G GRCh38
NC_000010.10:g.75830822C>G , CM000672.1:g.75830822C>G GRCh37
NC_000010.9:g.75500828C>G NCBI36
NG_008868.1:g.77951C>G , LRG_383:g.77951C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000211998.10:c.480C>G MANE Select ENSP00000211998.5:p.Tyr160Ter
ENST00000211998.8:c.480C>G ENSP00000211998.4:p.Tyr160Ter
ENST00000372755.7:c.480C>G ENSP00000361841.3:p.Tyr160Ter
ENST00000478896.2:n.331+27911C>G
ENST00000623461.3:n.438C>G
ENST00000624354.3:c.*235C>G ENSP00000485551.1:n.*235C>G
NM_003373.3:c.480C>G NP_003364.1:p.Tyr160Ter
NM_014000.2:c.480C>G , LRG_383t1:c.480C>G NP_054706.1:p.Tyr160Ter
XM_005270142.1:c.480C>G XP_005270199.1:p.Tyr160Ter
XM_005270143.1:c.480C>G XP_005270200.1:p.Tyr160Ter
NM_003373.4:c.480C>G NP_003364.1:p.Tyr160Ter
NM_014000.3:c.480C>G MANE Select NP_054706.1:p.Tyr160Ter