Canonical Allele Identifier: CA1583372465
Gene: AFF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132892200G= , CM000667.2:g.132892200G= GRCh38
NC_000005.9:g.132227892G= , CM000667.1:g.132227892G= GRCh37
NC_000005.8:g.132255791G= NCBI36
NG_030340.1:g.76463C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265343.10:c.2601C= MANE Select ENSP00000265343.5:p.Thr867=
ENST00000265343.9:c.2601C= ENSP00000265343.5:p.Thr867=
ENST00000378595.7:c.2601C= ENSP00000367858.3:p.Thr867=
NM_014423.3:c.2601C= NP_055238.1:p.Thr867=
XM_005271963.3:c.2601C= XP_005272020.1:p.Thr867=
XM_005271964.3:c.1467C= XP_005272021.1:p.Thr489=
XM_006714587.2:c.2514C= XP_006714650.1:p.Thr838=
XM_005271963.5:c.2601C= XP_005272020.1:p.Thr867=
XM_005271964.4:c.1467C= XP_005272021.1:p.Thr489=
XM_006714587.4:c.2514C= XP_006714650.1:p.Thr838=
NM_014423.4:c.2601C= MANE Select NP_055238.1:p.Thr867=