Canonical Allele Identifier: CA1139955321

Gene: VAV3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.107572523T= , CM000663.2:g.107572523T=	GRCh38
NC_000001.10:g.108115145T= , CM000663.1:g.108115145T=	GRCh37
NC_000001.9:g.107916668T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370056.9:c.*808A= MANE Select	ENSP00000359073.4:n.*808A=
ENST00000370056.8:c.*808A=	ENSP00000359073.4:n.*808A=
ENST00000527011.5:c.*808A=	ENSP00000432540.1:n.*808A=
NM_001079874.1:c.*808A=	NP_001073343.1:n.*808A=
NM_006113.4:c.*808A=	NP_006104.4:n.*808A=
XM_005270360.1:c.*808A=	XP_005270417.1:n.*808A=
XM_011540502.1:c.*808A=	XP_011538804.1:n.*808A=
XM_011540503.1:c.*808A=	XP_011538805.1:n.*808A=
XR_946522.1:n.3432A=
XM_005270360.2:c.*808A=	XP_005270417.1:n.*808A=
XM_017000053.1:c.*808A=	XP_016855542.1:n.*808A=
XM_017000055.1:c.*808A=	XP_016855544.1:n.*808A=
XM_017000056.1:c.*808A=	XP_016855545.1:n.*808A=
XM_024450319.1:c.*808A=	XP_024306087.1:n.*808A=
XR_001736913.1:n.3353A=
NM_006113.5:c.*808A= MANE Select	NP_006104.4:n.*808A=
NM_001079874.2:c.*808A=	NP_001073343.1:n.*808A=