Canonical Allele Identifier: CA1583396081
Gene: AFF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132934304G= , CM000667.2:g.132934304G= GRCh38
NC_000005.9:g.132269996G= , CM000667.1:g.132269996G= GRCh37
NC_000005.8:g.132297895G= NCBI36
NG_030340.1:g.34359C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265343.10:c.761C= MANE Select ENSP00000265343.5:p.Thr254=
ENST00000265343.9:c.761C= ENSP00000265343.5:p.Thr254=
ENST00000378595.7:c.761C= ENSP00000367858.3:p.Thr254=
ENST00000465484.1:n.1020C=
ENST00000491831.5:n.1021C=
NM_014423.3:c.761C= NP_055238.1:p.Thr254=
XM_005271963.3:c.761C= XP_005272020.1:p.Thr254=
XM_006714587.2:c.761C= XP_006714650.1:p.Thr254=
XM_005271963.5:c.761C= XP_005272020.1:p.Thr254=
XM_006714587.4:c.761C= XP_006714650.1:p.Thr254=
NM_014423.4:c.761C= MANE Select NP_055238.1:p.Thr254=