Canonical Allele Identifier: CA1187460075

Gene: VAV3

Linked Data

• dbSNP Id: rs7521681

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.107779913G>T , CM000663.2:g.107779913G>T	GRCh38
NC_000001.10:g.108322535G>T , CM000663.1:g.108322535G>T	GRCh37
NC_000001.9:g.108124058G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000370056.9:c.322-421C>A MANE Select	ENSP00000359073.4:n.322-421C>A
ENST00000343258.8:n.168-421C>A
ENST00000370056.8:c.322-421C>A	ENSP00000359073.4:n.322-421C>A
ENST00000469325.5:n.297-421C>A
ENST00000490388.2:c.306-421C>A
ENST00000524574.5:n.112-421C>A
ENST00000527011.5:c.322-421C>A	ENSP00000432540.1:n.322-421C>A
ENST00000530671.1:n.272-421C>A
NM_006113.4:c.322-421C>A	NP_006104.4:n.322-421C>A
XM_005270360.1:c.40-421C>A	XP_005270417.1:n.40-421C>A
XM_005270361.1:c.322-421C>A	XP_005270418.1:n.322-421C>A
XM_011540502.1:c.370-421C>A	XP_011538804.1:n.370-421C>A
XM_011540503.1:c.370-421C>A	XP_011538805.1:n.370-421C>A
XM_011540504.1:c.370-421C>A	XP_011538806.1:n.370-421C>A
XM_011540505.1:c.370-421C>A	XP_011538807.1:n.370-421C>A
XM_011540506.1:c.370-421C>A	XP_011538808.1:n.370-421C>A
XR_946522.1:n.448-421C>A
XM_005270360.2:c.40-421C>A	XP_005270417.1:n.40-421C>A
XM_017000053.1:c.322-421C>A	XP_016855542.1:n.322-421C>A
XM_017000054.1:c.322-421C>A	XP_016855543.1:n.322-421C>A
XM_017000055.1:c.34-421C>A	XP_016855544.1:n.34-421C>A
XM_024450319.1:c.61-421C>A	XP_024306087.1:n.61-421C>A
XR_001736913.1:n.369-421C>A
NM_006113.5:c.322-421C>A MANE Select	NP_006104.4:n.322-421C>A