Canonical Allele Identifier: CA1583396039
Gene: AFF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132934197T= , CM000667.2:g.132934197T= GRCh38
NC_000005.9:g.132269889T= , CM000667.1:g.132269889T= GRCh37
NC_000005.8:g.132297788T= NCBI36
NG_030340.1:g.34466A=

Transcript Alleles

HGVS Amino-acid change
ENST00000265343.10:c.868A= MANE Select ENSP00000265343.5:p.Ser290=
ENST00000265343.9:c.868A= ENSP00000265343.5:p.Ser290=
ENST00000378593.6:n.35A=
ENST00000378595.7:c.868A= ENSP00000367858.3:p.Ser290=
ENST00000425658.1:c.42A=
ENST00000465484.1:n.1127A=
ENST00000491831.5:n.1128A=
NM_014423.3:c.868A= NP_055238.1:p.Ser290=
XM_005271963.3:c.868A= XP_005272020.1:p.Ser290=
XM_006714587.2:c.868A= XP_006714650.1:p.Ser290=
XM_005271963.5:c.868A= XP_005272020.1:p.Ser290=
XM_006714587.4:c.868A= XP_006714650.1:p.Ser290=
NM_014423.4:c.868A= MANE Select NP_055238.1:p.Ser290=