Canonical Allele Identifier: CA470172301

Gene: VCL

Linked Data

• MyVariant Identifiers: chr10:g.75848984G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74089226G>A , CM000672.2:g.74089226G>A	GRCh38
NC_000010.10:g.75848984G>A , CM000672.1:g.75848984G>A	GRCh37
NC_000010.9:g.75518990G>A	NCBI36
NG_008868.1:g.96113G>A , LRG_383:g.96113G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000211998.10:c.1053G>A MANE Select	ENSP00000211998.5:p.Gln351=
ENST00000211998.8:c.1053G>A	ENSP00000211998.4:p.Gln351=
ENST00000372755.7:c.1053G>A	ENSP00000361841.3:p.Gln351=
ENST00000436396.1:c.69G>A	ENSP00000415489.1:p.Gln23=
ENST00000478896.2:n.332-11828G>A
ENST00000623461.3:n.3856G>A
ENST00000624354.3:c.*808G>A	ENSP00000485551.1:n.*808G>A
NM_003373.3:c.1053G>A	NP_003364.1:p.Gln351=
NM_014000.2:c.1053G>A , LRG_383t1:c.1053G>A	NP_054706.1:p.Gln351=
XM_005270142.1:c.1056G>A	XP_005270199.1:p.Gln352=
XM_005270143.1:c.1056G>A	XP_005270200.1:p.Gln352=
XR_001747501.1:n.89+706C>T
NM_003373.4:c.1053G>A	NP_003364.1:p.Gln351=
NM_014000.3:c.1053G>A MANE Select	NP_054706.1:p.Gln351=