Canonical Allele Identifier: CA470171155

Gene: VCL

Linked Data

• MyVariant Identifiers: chr10:g.75842259G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74082501G>A , CM000672.2:g.74082501G>A	GRCh38
NC_000010.10:g.75842259G>A , CM000672.1:g.75842259G>A	GRCh37
NC_000010.9:g.75512265G>A	NCBI36
NG_008868.1:g.89388G>A , LRG_383:g.89388G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.831G>A MANE Select	ENSP00000211998.5:p.Leu277=
ENST00000211998.8:c.831G>A	ENSP00000211998.4:p.Leu277=
ENST00000372755.7:c.831G>A	ENSP00000361841.3:p.Leu277=
ENST00000478896.2:n.332-18553G>A
ENST00000623461.3:n.3634G>A
ENST00000624354.3:c.*586G>A	ENSP00000485551.1:n.*586G>A
NM_003373.3:c.831G>A	NP_003364.1:p.Leu277=
NM_014000.2:c.831G>A , LRG_383t1:c.831G>A	NP_054706.1:p.Leu277=
XM_005270142.1:c.834G>A	XP_005270199.1:p.Leu278=
XM_005270143.1:c.834G>A	XP_005270200.1:p.Leu278=
XR_001747501.1:n.90-4774C>T
NM_003373.4:c.831G>A	NP_003364.1:p.Leu277=
NM_014000.3:c.831G>A MANE Select	NP_054706.1:p.Leu277=