Canonical Allele Identifier: CA2034925852
Gene: ARF3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48939763G= , CM000674.2:g.48939763G= GRCh38
NC_000012.11:g.49333546G= , CM000674.1:g.49333546G= GRCh37
NC_000012.10:g.47619813G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256682.9:c.276C= MANE Select ENSP00000256682.4:p.Val92=
ENST00000256682.8:c.276C= ENSP00000256682.4:p.Val92=
ENST00000398092.4:c.276C= ENSP00000438507.1:p.Val92=
ENST00000447318.6:c.165C= ENSP00000395370.2:p.Val55=
ENST00000485410.5:n.137-916C=
ENST00000541236.5:c.276C= ENSP00000438063.1:p.Val92=
ENST00000541959.5:c.276C= ENSP00000438510.1:p.Val92=
NM_001659.2:c.276C= NP_001650.1:p.Val92=
XM_005268856.1:c.276C= XP_005268913.1:p.Val92=
XM_006719391.2:c.276C= XP_006719454.1:p.Val92=
XM_011538322.1:c.276C= XP_011536624.1:p.Val92=
XM_011538323.1:c.276C= XP_011536625.1:p.Val92=
XM_006719391.4:c.276C= XP_006719454.1:p.Val92=
XM_024448972.1:c.276C= XP_024304740.1:p.Val92=
NM_001659.3:c.276C= MANE Select NP_001650.1:p.Val92=