Canonical Allele Identifier: CA377277664

Gene: VCL

Linked Data

• MyVariant Identifiers: chr10:g.75860761C>G (hg19) ; chr10:g.74101003C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74101003C>G , CM000672.2:g.74101003C>G	GRCh38
NC_000010.10:g.75860761C>G , CM000672.1:g.75860761C>G	GRCh37
NC_000010.9:g.75530767C>G	NCBI36
NG_008868.1:g.107890C>G , LRG_383:g.107890C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.1928C>G MANE Select	ENSP00000211998.5:p.Thr643Arg
ENST00000211998.8:c.1928C>G	ENSP00000211998.4:p.Thr643Arg
ENST00000372755.7:c.1928C>G	ENSP00000361841.3:p.Thr643Arg
ENST00000436396.1:c.944C>G	ENSP00000415489.1:p.Thr315Arg
ENST00000478896.2:n.332-51C>G
ENST00000623461.3:n.4731C>G
ENST00000624354.3:c.*1683C>G	ENSP00000485551.1:n.*1683C>G
NM_003373.3:c.1928C>G	NP_003364.1:p.Thr643Arg
NM_014000.2:c.1928C>G , LRG_383t1:c.1928C>G	NP_054706.1:p.Thr643Arg
XM_005270142.1:c.1931C>G	XP_005270199.1:p.Thr644Arg
XM_005270143.1:c.1931C>G	XP_005270200.1:p.Thr644Arg
NM_003373.4:c.1928C>G	NP_003364.1:p.Thr643Arg
NM_014000.3:c.1928C>G MANE Select	NP_054706.1:p.Thr643Arg