Canonical Allele Identifier: CA377264804

Gene: VCL

Linked Data

• dbSNP Id: rs1488842009
• gnomAD v3: 10-74112048-T-C
• gnomAD v4: 10-74112048-T-C
• MyVariant Identifiers: chr10:g.75871806T>C (hg19) ; chr10:g.74112048T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74112048T>C , CM000672.2:g.74112048T>C	GRCh38
NC_000010.10:g.75871806T>C , CM000672.1:g.75871806T>C	GRCh37
NC_000010.9:g.75541812T>C	NCBI36
NG_008868.1:g.118935T>C , LRG_383:g.118935T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.2885T>C MANE Select	ENSP00000211998.5:p.Val962Ala
ENST00000211998.8:c.2885T>C	ENSP00000211998.4:p.Val962Ala
ENST00000372755.7:c.2746-2136T>C	ENSP00000361841.3:n.2746-2136T>C
ENST00000436396.1:c.1901T>C	ENSP00000415489.1:p.Val634Ala
ENST00000623461.3:n.5549-2136T>C
ENST00000624354.3:c.*2640T>C	ENSP00000485551.1:n.*2640T>C
NM_003373.3:c.2746-2136T>C	NP_003364.1:n.2746-2136T>C
NM_014000.2:c.2885T>C , LRG_383t1:c.2885T>C	NP_054706.1:p.Val962Ala
XM_005270142.1:c.2888T>C	XP_005270199.1:p.Val963Ala
XM_005270143.1:c.2749-2136T>C	XP_005270200.1:n.2749-2136T>C
NM_003373.4:c.2746-2136T>C	NP_003364.1:n.2746-2136T>C
NM_014000.3:c.2885T>C MANE Select	NP_054706.1:p.Val962Ala