Canonical Allele Identifier: CA1583396082
Gene: AFF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132934305T= , CM000667.2:g.132934305T= GRCh38
NC_000005.9:g.132269997T= , CM000667.1:g.132269997T= GRCh37
NC_000005.8:g.132297896T= NCBI36
NG_030340.1:g.34358A=

Transcript Alleles

HGVS Amino-acid change
ENST00000265343.10:c.760A= MANE Select ENSP00000265343.5:p.Thr254=
ENST00000265343.9:c.760A= ENSP00000265343.5:p.Thr254=
ENST00000378595.7:c.760A= ENSP00000367858.3:p.Thr254=
ENST00000465484.1:n.1019A=
ENST00000491831.5:n.1020A=
NM_014423.3:c.760A= NP_055238.1:p.Thr254=
XM_005271963.3:c.760A= XP_005272020.1:p.Thr254=
XM_006714587.2:c.760A= XP_006714650.1:p.Thr254=
XM_005271963.5:c.760A= XP_005272020.1:p.Thr254=
XM_006714587.4:c.760A= XP_006714650.1:p.Thr254=
NM_014423.4:c.760A= MANE Select NP_055238.1:p.Thr254=