Canonical Allele Identifier: CA1583372471
Gene: AFF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132892220T= , CM000667.2:g.132892220T= GRCh38
NC_000005.9:g.132227912T= , CM000667.1:g.132227912T= GRCh37
NC_000005.8:g.132255811T= NCBI36
NG_030340.1:g.76443A=

Transcript Alleles

HGVS Amino-acid change
ENST00000265343.10:c.2581A= MANE Select ENSP00000265343.5:p.Thr861=
ENST00000265343.9:c.2581A= ENSP00000265343.5:p.Thr861=
ENST00000378595.7:c.2581A= ENSP00000367858.3:p.Thr861=
NM_014423.3:c.2581A= NP_055238.1:p.Thr861=
XM_005271963.3:c.2581A= XP_005272020.1:p.Thr861=
XM_005271964.3:c.1447A= XP_005272021.1:p.Thr483=
XM_006714587.2:c.2494A= XP_006714650.1:p.Thr832=
XM_005271963.5:c.2581A= XP_005272020.1:p.Thr861=
XM_005271964.4:c.1447A= XP_005272021.1:p.Thr483=
XM_006714587.4:c.2494A= XP_006714650.1:p.Thr832=
NM_014423.4:c.2581A= MANE Select NP_055238.1:p.Thr861=