Canonical Allele Identifier: CA377264797

Gene: VCL

Linked Data

• dbSNP Id: rs1316850168
• gnomAD v2: 10-75871802-C-G
• gnomAD v4: 10-74112044-C-G
• MyVariant Identifiers: chr10:g.75871802C>G (hg19) ; chr10:g.74112044C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74112044C>G , CM000672.2:g.74112044C>G	GRCh38
NC_000010.10:g.75871802C>G , CM000672.1:g.75871802C>G	GRCh37
NC_000010.9:g.75541808C>G	NCBI36
NG_008868.1:g.118931C>G , LRG_383:g.118931C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.2881C>G MANE Select	ENSP00000211998.5:p.Pro961Ala
ENST00000211998.8:c.2881C>G	ENSP00000211998.4:p.Pro961Ala
ENST00000372755.7:c.2746-2140C>G	ENSP00000361841.3:n.2746-2140C>G
ENST00000436396.1:c.1897C>G	ENSP00000415489.1:p.Pro633Ala
ENST00000623461.3:n.5549-2140C>G
ENST00000624354.3:c.*2636C>G	ENSP00000485551.1:n.*2636C>G
NM_003373.3:c.2746-2140C>G	NP_003364.1:n.2746-2140C>G
NM_014000.2:c.2881C>G , LRG_383t1:c.2881C>G	NP_054706.1:p.Pro961Ala
XM_005270142.1:c.2884C>G	XP_005270199.1:p.Pro962Ala
XM_005270143.1:c.2749-2140C>G	XP_005270200.1:n.2749-2140C>G
NM_003373.4:c.2746-2140C>G	NP_003364.1:n.2746-2140C>G
NM_014000.3:c.2881C>G MANE Select	NP_054706.1:p.Pro961Ala