Canonical Allele Identifier: CA470166529

Gene: VCL

Linked Data

• ClinVar Variation Id: 1629696
• ClinVar RCV Id: RCV002125571 ; RCV002337341
• dbSNP Id: rs2136272917
• MyVariant Identifiers: chr10:g.75830822C>T (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.480C>T MANE Select	ENSP00000211998.5:p.Tyr160=
ENST00000211998.8:c.480C>T	ENSP00000211998.4:p.Tyr160=
ENST00000372755.7:c.480C>T	ENSP00000361841.3:p.Tyr160=
ENST00000478896.2:n.331+27911C>T
ENST00000623461.3:n.438C>T
ENST00000624354.3:c.*235C>T	ENSP00000485551.1:n.*235C>T
NM_003373.3:c.480C>T	NP_003364.1:p.Tyr160=
NM_014000.2:c.480C>T , LRG_383t1:c.480C>T	NP_054706.1:p.Tyr160=
XM_005270142.1:c.480C>T	XP_005270199.1:p.Tyr160=
XM_005270143.1:c.480C>T	XP_005270200.1:p.Tyr160=
NM_003373.4:c.480C>T	NP_003364.1:p.Tyr160=
NM_014000.3:c.480C>T MANE Select	NP_054706.1:p.Tyr160=