Canonical Allele Identifier: CA1583372529
Gene: AFF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132892373C= , CM000667.2:g.132892373C= GRCh38
NC_000005.9:g.132228065C= , CM000667.1:g.132228065C= GRCh37
NC_000005.8:g.132255964C= NCBI36
NG_030340.1:g.76290G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265343.10:c.2428G= MANE Select ENSP00000265343.5:p.Asp810=
ENST00000265343.9:c.2428G= ENSP00000265343.5:p.Asp810=
ENST00000378595.7:c.2428G= ENSP00000367858.3:p.Asp810=
NM_014423.3:c.2428G= NP_055238.1:p.Asp810=
XM_005271963.3:c.2428G= XP_005272020.1:p.Asp810=
XM_005271964.3:c.1294G= XP_005272021.1:p.Asp432=
XM_006714587.2:c.2341G= XP_006714650.1:p.Asp781=
XM_005271963.5:c.2428G= XP_005272020.1:p.Asp810=
XM_005271964.4:c.1294G= XP_005272021.1:p.Asp432=
XM_006714587.4:c.2341G= XP_006714650.1:p.Asp781=
NM_014423.4:c.2428G= MANE Select NP_055238.1:p.Asp810=