Canonical Allele Identifier: CA1882871478
Gene: VAV2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133855609G= , CM000671.2:g.133855609G= GRCh38
NC_000009.11:g.136720731G= , CM000671.1:g.136720731G= GRCh37
NC_000009.10:g.135710552G= NCBI36
NG_029725.1:g.141716C=

Transcript Alleles

HGVS Amino-acid change
ENST00000371850.8:c.380+5765C= MANE Select ENSP00000360916.3:n.380+5765C=
ENST00000371850.7:c.380+5765C= ENSP00000360916.3:n.380+5765C=
ENST00000371851.1:c.380+5765C= ENSP00000360917.1:n.380+5765C=
ENST00000406606.7:c.380+5765C= ENSP00000385362.3:n.380+5765C=
NM_001134398.1:c.380+5765C= NP_001127870.1:n.380+5765C=
NM_003371.3:c.380+5765C= NP_003362.2:n.380+5765C=
XM_005272213.1:c.380+5765C= XP_005272270.1:n.380+5765C=
XM_006717277.1:c.380+5765C= XP_006717340.1:n.380+5765C=
XM_011518983.1:c.380+5765C= XP_011517285.1:n.380+5765C=
XM_011518984.1:c.380+5765C= XP_011517286.1:n.380+5765C=
XM_017015108.1:c.380+5765C= XP_016870597.1:n.380+5765C=
XM_017015109.1:c.380+5765C= XP_016870598.1:n.380+5765C=
XM_017015110.1:c.380+5765C= XP_016870599.1:n.380+5765C=
XM_017015111.1:c.380+5765C= XP_016870600.1:n.380+5765C=
XM_017015112.1:c.380+5765C= XP_016870601.1:n.380+5765C=
XM_017015113.1:c.380+5765C= XP_016870602.1:n.380+5765C=
NM_001134398.2:c.380+5765C= MANE Select NP_001127870.1:n.380+5765C=
NM_003371.4:c.380+5765C= NP_003362.2:n.380+5765C=