Canonical Allele Identifier: CA1187477692

Gene: VAV3

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.107823394T>G , CM000663.2:g.107823394T>G	GRCh38
NC_000001.10:g.108366016T>G , CM000663.1:g.108366016T>G	GRCh37
NC_000001.9:g.108167539T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370056.9:c.322-43902A>C MANE Select	ENSP00000359073.4:n.322-43902A>C
ENST00000370056.8:c.322-43902A>C	ENSP00000359073.4:n.322-43902A>C
ENST00000469325.5:n.297-43902A>C
ENST00000490388.2:c.306-43902A>C
ENST00000527011.5:c.322-43902A>C	ENSP00000432540.1:n.322-43902A>C
ENST00000530671.1:n.271+39290A>C
NM_006113.4:c.322-43902A>C	NP_006104.4:n.322-43902A>C
XM_005270361.1:c.322-43902A>C	XP_005270418.1:n.322-43902A>C
XM_011540502.1:c.370-43902A>C	XP_011538804.1:n.370-43902A>C
XM_011540503.1:c.370-43902A>C	XP_011538805.1:n.370-43902A>C
XM_011540504.1:c.370-43902A>C	XP_011538806.1:n.370-43902A>C
XM_011540505.1:c.370-43902A>C	XP_011538807.1:n.370-43902A>C
XM_011540506.1:c.370-43902A>C	XP_011538808.1:n.370-43902A>C
XR_946522.1:n.448-43902A>C
XM_017000053.1:c.322-43902A>C	XP_016855542.1:n.322-43902A>C
XM_017000054.1:c.322-43902A>C	XP_016855543.1:n.322-43902A>C
XM_024450319.1:c.61-43902A>C	XP_024306087.1:n.61-43902A>C
XR_001736913.1:n.369-43902A>C
NM_006113.5:c.322-43902A>C MANE Select	NP_006104.4:n.322-43902A>C