Canonical Allele Identifier: CA1583396079
Gene: AFF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132934300G= , CM000667.2:g.132934300G= GRCh38
NC_000005.9:g.132269992G= , CM000667.1:g.132269992G= GRCh37
NC_000005.8:g.132297891G= NCBI36
NG_030340.1:g.34363C=

Transcript Alleles

HGVS Amino-acid change
ENST00000265343.10:c.765C= MANE Select ENSP00000265343.5:p.Ala255=
ENST00000265343.9:c.765C= ENSP00000265343.5:p.Ala255=
ENST00000378595.7:c.765C= ENSP00000367858.3:p.Ala255=
ENST00000465484.1:n.1024C=
ENST00000491831.5:n.1025C=
NM_014423.3:c.765C= NP_055238.1:p.Ala255=
XM_005271963.3:c.765C= XP_005272020.1:p.Ala255=
XM_006714587.2:c.765C= XP_006714650.1:p.Ala255=
XM_005271963.5:c.765C= XP_005272020.1:p.Ala255=
XM_006714587.4:c.765C= XP_006714650.1:p.Ala255=
NM_014423.4:c.765C= MANE Select NP_055238.1:p.Ala255=