Canonical Allele Identifier: CA1583372535
Gene: AFF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132892385C= , CM000667.2:g.132892385C= GRCh38
NC_000005.9:g.132228077C= , CM000667.1:g.132228077C= GRCh37
NC_000005.8:g.132255976C= NCBI36
NG_030340.1:g.76278G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265343.10:c.2416G= MANE Select ENSP00000265343.5:p.Ala806=
ENST00000265343.9:c.2416G= ENSP00000265343.5:p.Ala806=
ENST00000378595.7:c.2416G= ENSP00000367858.3:p.Ala806=
NM_014423.3:c.2416G= NP_055238.1:p.Ala806=
XM_005271963.3:c.2416G= XP_005272020.1:p.Ala806=
XM_005271964.3:c.1282G= XP_005272021.1:p.Ala428=
XM_006714587.2:c.2329G= XP_006714650.1:p.Ala777=
XM_005271963.5:c.2416G= XP_005272020.1:p.Ala806=
XM_005271964.4:c.1282G= XP_005272021.1:p.Ala428=
XM_006714587.4:c.2329G= XP_006714650.1:p.Ala777=
NM_014423.4:c.2416G= MANE Select NP_055238.1:p.Ala806=