Allele Registry

Canonical Allele Identifier: CA273521

Gene: VCL HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr10:g.74097222C>T

GRCh37 chr10:g.75856980C>T

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000154540

ClinVar Variation:

177889

dbSNP:

727504381

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74097222C>T , CM000672.2:g.74097222C>T	GRCh38
NC_000010.10:g.75856980C>T , CM000672.1:g.75856980C>T	GRCh37
NC_000010.9:g.75526986C>T	NCBI36
NG_008868.1:g.104109C>T , LRG_383:g.104109C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.1762C>T MANE Select	ENSP00000211998.5:p.Gln588Ter
ENST00000211998.8:c.1762C>T	ENSP00000211998.4:p.Gln588Ter
ENST00000372755.7:c.1762C>T	ENSP00000361841.3:p.Gln588Ter
ENST00000436396.1:c.778C>T	ENSP00000415489.1:p.Gln260Ter
ENST00000478896.2:n.332-3832C>T
ENST00000623461.3:n.4565C>T
ENST00000624354.3:c.*1517C>T	ENSP00000485551.1:n.*1517C>T
NM_003373.3:c.1762C>T	NP_003364.1:p.Gln588Ter
NM_014000.2:c.1762C>T , LRG_383t1:c.1762C>T	NP_054706.1:p.Gln588Ter
XM_005270142.1:c.1765C>T	XP_005270199.1:p.Gln589Ter
XM_005270143.1:c.1765C>T	XP_005270200.1:p.Gln589Ter
NM_003373.4:c.1762C>T	NP_003364.1:p.Gln588Ter
NM_014000.3:c.1762C>T MANE Select	NP_054706.1:p.Gln588Ter

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