Canonical Allele Identifier: CA377277683

Gene: VCL

Linked Data

• MyVariant Identifiers: chr10:g.75860764C>T (hg19) ; chr10:g.74101006C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74101006C>T , CM000672.2:g.74101006C>T	GRCh38
NC_000010.10:g.75860764C>T , CM000672.1:g.75860764C>T	GRCh37
NC_000010.9:g.75530770C>T	NCBI36
NG_008868.1:g.107893C>T , LRG_383:g.107893C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000211998.10:c.1931C>T MANE Select	ENSP00000211998.5:p.Ala644Val
ENST00000211998.8:c.1931C>T	ENSP00000211998.4:p.Ala644Val
ENST00000372755.7:c.1931C>T	ENSP00000361841.3:p.Ala644Val
ENST00000436396.1:c.947C>T	ENSP00000415489.1:p.Ala316Val
ENST00000478896.2:n.332-48C>T
ENST00000623461.3:n.4734C>T
ENST00000624354.3:c.*1686C>T	ENSP00000485551.1:n.*1686C>T
NM_003373.3:c.1931C>T	NP_003364.1:p.Ala644Val
NM_014000.2:c.1931C>T , LRG_383t1:c.1931C>T	NP_054706.1:p.Ala644Val
XM_005270142.1:c.1934C>T	XP_005270199.1:p.Ala645Val
XM_005270143.1:c.1934C>T	XP_005270200.1:p.Ala645Val
NM_003373.4:c.1931C>T	NP_003364.1:p.Ala644Val
NM_014000.3:c.1931C>T MANE Select	NP_054706.1:p.Ala644Val