Canonical Allele Identifier: CA377269825

Gene: VCL

Linked Data

• MyVariant Identifiers: chr10:g.75842294C>A (hg19) ; chr10:g.74082536C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74082536C>A , CM000672.2:g.74082536C>A	GRCh38
NC_000010.10:g.75842294C>A , CM000672.1:g.75842294C>A	GRCh37
NC_000010.9:g.75512300C>A	NCBI36
NG_008868.1:g.89423C>A , LRG_383:g.89423C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.866C>A MANE Select	ENSP00000211998.5:p.Ala289Asp
ENST00000211998.8:c.866C>A	ENSP00000211998.4:p.Ala289Asp
ENST00000372755.7:c.866C>A	ENSP00000361841.3:p.Ala289Asp
ENST00000478896.2:n.332-18518C>A
ENST00000623461.3:n.3669C>A
ENST00000624354.3:c.*621C>A	ENSP00000485551.1:n.*621C>A
NM_003373.3:c.866C>A	NP_003364.1:p.Ala289Asp
NM_014000.2:c.866C>A , LRG_383t1:c.866C>A	NP_054706.1:p.Ala289Asp
XM_005270142.1:c.869C>A	XP_005270199.1:p.Ala290Asp
XM_005270143.1:c.869C>A	XP_005270200.1:p.Ala290Asp
XR_001747501.1:n.90-4809G>T
NM_003373.4:c.866C>A	NP_003364.1:p.Ala289Asp
NM_014000.3:c.866C>A MANE Select	NP_054706.1:p.Ala289Asp