Canonical Allele Identifier: CA1005514523
Gene: VAV3 HGNC NCBI

Linked Data

dbSNP Id: rs1665595090

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.107779882T>A , CM000663.2:g.107779882T>A GRCh38
NC_000001.10:g.108322504T>A , CM000663.1:g.108322504T>A GRCh37
NC_000001.9:g.108124027T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000370056.9:c.322-390A>T MANE Select ENSP00000359073.4:n.322-390A>T
ENST00000343258.8:n.168-390A>T
ENST00000370056.8:c.322-390A>T ENSP00000359073.4:n.322-390A>T
ENST00000469325.5:n.297-390A>T
ENST00000490388.2:c.306-390A>T
ENST00000524574.5:n.112-390A>T
ENST00000527011.5:c.322-390A>T ENSP00000432540.1:n.322-390A>T
ENST00000530671.1:n.272-390A>T
NM_006113.4:c.322-390A>T NP_006104.4:n.322-390A>T
XM_005270360.1:c.40-390A>T XP_005270417.1:n.40-390A>T
XM_005270361.1:c.322-390A>T XP_005270418.1:n.322-390A>T
XM_011540502.1:c.370-390A>T XP_011538804.1:n.370-390A>T
XM_011540503.1:c.370-390A>T XP_011538805.1:n.370-390A>T
XM_011540504.1:c.370-390A>T XP_011538806.1:n.370-390A>T
XM_011540505.1:c.370-390A>T XP_011538807.1:n.370-390A>T
XM_011540506.1:c.370-390A>T XP_011538808.1:n.370-390A>T
XR_946522.1:n.448-390A>T
XM_005270360.2:c.40-390A>T XP_005270417.1:n.40-390A>T
XM_017000053.1:c.322-390A>T XP_016855542.1:n.322-390A>T
XM_017000054.1:c.322-390A>T XP_016855543.1:n.322-390A>T
XM_017000055.1:c.34-390A>T XP_016855544.1:n.34-390A>T
XM_024450319.1:c.61-390A>T XP_024306087.1:n.61-390A>T
XR_001736913.1:n.369-390A>T
NM_006113.5:c.322-390A>T MANE Select NP_006104.4:n.322-390A>T