Canonical Allele Identifier: CA470166528

Gene: VCL

Linked Data

• MyVariant Identifiers: chr10:g.75830819T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74071061T>G , CM000672.2:g.74071061T>G	GRCh38
NC_000010.10:g.75830819T>G , CM000672.1:g.75830819T>G	GRCh37
NC_000010.9:g.75500825T>G	NCBI36
NG_008868.1:g.77948T>G , LRG_383:g.77948T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.477T>G MANE Select	ENSP00000211998.5:p.Thr159=
ENST00000211998.8:c.477T>G	ENSP00000211998.4:p.Thr159=
ENST00000372755.7:c.477T>G	ENSP00000361841.3:p.Thr159=
ENST00000478896.2:n.331+27908T>G
ENST00000623461.3:n.435T>G
ENST00000624354.3:c.*232T>G	ENSP00000485551.1:n.*232T>G
NM_003373.3:c.477T>G	NP_003364.1:p.Thr159=
NM_014000.2:c.477T>G , LRG_383t1:c.477T>G	NP_054706.1:p.Thr159=
XM_005270142.1:c.477T>G	XP_005270199.1:p.Thr159=
XM_005270143.1:c.477T>G	XP_005270200.1:p.Thr159=
NM_003373.4:c.477T>G	NP_003364.1:p.Thr159=
NM_014000.3:c.477T>G MANE Select	NP_054706.1:p.Thr159=