Canonical Allele Identifier: CA1882944701

Gene: VAV2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133970221A= , CM000671.2:g.133970221A=	GRCh38
NC_000009.11:g.136835343A= , CM000671.1:g.136835343A=	GRCh37
NC_000009.10:g.135825164A=	NCBI36
NG_029725.1:g.27104T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001134398.2:c.204+21854T= MANE Select	NP_001127870.1:n.204+21854T=
ENST00000371850.8:c.204+21854T= MANE Select	ENSP00000360916.3:n.204+21854T=
NM_001134398.1:c.204+21854T=	NP_001127870.1:n.204+21854T=
NM_003371.3:c.204+21854T=	NP_003362.2:n.204+21854T=
NM_003371.4:c.204+21854T=	NP_003362.2:n.204+21854T=
ENST00000371850.7:c.204+21854T=	ENSP00000360916.3:n.204+21854T=
ENST00000371851.1:c.204+21854T=	ENSP00000360917.1:n.204+21854T=
ENST00000406606.7:c.204+21854T=	ENSP00000385362.3:n.204+21854T=
ENST00000486113.1:n.185+21854T=
XM_005272213.1:c.204+21854T=	XP_005272270.1:n.204+21854T=
XM_006717277.1:c.204+21854T=	XP_006717340.1:n.204+21854T=
XM_011518983.1:c.204+21854T=	XP_011517285.1:n.204+21854T=
XM_011518984.1:c.204+21854T=	XP_011517286.1:n.204+21854T=
XM_017015108.1:c.204+21854T=	XP_016870597.1:n.204+21854T=
XM_017015109.1:c.204+21854T=	XP_016870598.1:n.204+21854T=
XM_017015110.1:c.204+21854T=	XP_016870599.1:n.204+21854T=
XM_017015111.1:c.204+21854T=	XP_016870600.1:n.204+21854T=
XM_017015112.1:c.204+21854T=	XP_016870601.1:n.204+21854T=
XM_017015113.1:c.204+21854T=	XP_016870602.1:n.204+21854T=