Canonical Allele Identifier: CA377269759

Gene: VCL

Linked Data

• MyVariant Identifiers: chr10:g.75842284G>A (hg19) ; chr10:g.74082526G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74082526G>A , CM000672.2:g.74082526G>A	GRCh38
NC_000010.10:g.75842284G>A , CM000672.1:g.75842284G>A	GRCh37
NC_000010.9:g.75512290G>A	NCBI36
NG_008868.1:g.89413G>A , LRG_383:g.89413G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.856G>A MANE Select	ENSP00000211998.5:p.Asp286Asn
ENST00000211998.8:c.856G>A	ENSP00000211998.4:p.Asp286Asn
ENST00000372755.7:c.856G>A	ENSP00000361841.3:p.Asp286Asn
ENST00000478896.2:n.332-18528G>A
ENST00000623461.3:n.3659G>A
ENST00000624354.3:c.*611G>A	ENSP00000485551.1:n.*611G>A
NM_003373.3:c.856G>A	NP_003364.1:p.Asp286Asn
NM_014000.2:c.856G>A , LRG_383t1:c.856G>A	NP_054706.1:p.Asp286Asn
XM_005270142.1:c.859G>A	XP_005270199.1:p.Asp287Asn
XM_005270143.1:c.859G>A	XP_005270200.1:p.Asp287Asn
XR_001747501.1:n.90-4799C>T
NM_003373.4:c.856G>A	NP_003364.1:p.Asp286Asn
NM_014000.3:c.856G>A MANE Select	NP_054706.1:p.Asp286Asn