Canonical Allele Identifier: CA377264846

Gene: VCL

Linked Data

• MyVariant Identifiers: chr10:g.75871827C>G (hg19) ; chr10:g.74112069C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74112069C>G , CM000672.2:g.74112069C>G	GRCh38
NC_000010.10:g.75871827C>G , CM000672.1:g.75871827C>G	GRCh37
NC_000010.9:g.75541833C>G	NCBI36
NG_008868.1:g.118956C>G , LRG_383:g.118956C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000211998.10:c.2906C>G MANE Select	ENSP00000211998.5:p.Ala969Gly
ENST00000211998.8:c.2906C>G	ENSP00000211998.4:p.Ala969Gly
ENST00000372755.7:c.2746-2115C>G	ENSP00000361841.3:n.2746-2115C>G
ENST00000436396.1:c.1922C>G	ENSP00000415489.1:p.Ala641Gly
ENST00000623461.3:n.5549-2115C>G
ENST00000624354.3:c.*2661C>G	ENSP00000485551.1:n.*2661C>G
NM_003373.3:c.2746-2115C>G	NP_003364.1:n.2746-2115C>G
NM_014000.2:c.2906C>G , LRG_383t1:c.2906C>G	NP_054706.1:p.Ala969Gly
XM_005270142.1:c.2909C>G	XP_005270199.1:p.Ala970Gly
XM_005270143.1:c.2749-2115C>G	XP_005270200.1:n.2749-2115C>G
NM_003373.4:c.2746-2115C>G	NP_003364.1:n.2746-2115C>G
NM_014000.3:c.2906C>G MANE Select	NP_054706.1:p.Ala969Gly