Canonical Allele Identifier: CA15146522

Gene: VAV3

Linked Data

• dbSNP Id: rs345299
• gnomAD v2: 1-108448133-A-C
• gnomAD v3: 1-107905511-A-C
• gnomAD v4: 1-107905511-A-C
• MyVariant Identifiers: chr1:g.108448133A>C (hg19) ; chr1:g.107905511A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.107905511A>C , CM000663.2:g.107905511A>C	GRCh38
NC_000001.10:g.108448133A>C , CM000663.1:g.108448133A>C	GRCh37
NC_000001.9:g.108249656A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000370056.9:c.205-30494T>G MANE Select	ENSP00000359073.4:n.205-30494T>G
ENST00000370056.8:c.205-30494T>G	ENSP00000359073.4:n.205-30494T>G
ENST00000469325.5:n.180-30494T>G
ENST00000490388.2:c.189-30494T>G
ENST00000527011.5:c.205-30494T>G	ENSP00000432540.1:n.205-30494T>G
ENST00000530671.1:n.84-30494T>G
NM_006113.4:c.205-30494T>G	NP_006104.4:n.205-30494T>G
XM_005270361.1:c.205-30494T>G	XP_005270418.1:n.205-30494T>G
XM_011540502.1:c.253-30494T>G	XP_011538804.1:n.253-30494T>G
XM_011540503.1:c.253-30494T>G	XP_011538805.1:n.253-30494T>G
XM_011540504.1:c.253-30494T>G	XP_011538806.1:n.253-30494T>G
XM_011540505.1:c.253-30494T>G	XP_011538807.1:n.253-30494T>G
XM_011540506.1:c.253-30494T>G	XP_011538808.1:n.253-30494T>G
XR_946522.1:n.331-30494T>G
XM_017000053.1:c.205-30494T>G	XP_016855542.1:n.205-30494T>G
XM_017000054.1:c.205-30494T>G	XP_016855543.1:n.205-30494T>G
XM_024450319.1:c.-57-30494T>G	XP_024306087.1:n.-57-30494T>G
XR_001736913.1:n.252-30494T>G
NM_006113.5:c.205-30494T>G MANE Select	NP_006104.4:n.205-30494T>G