Canonical Allele Identifier: CA1583372507
Gene: AFF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132892310G= , CM000667.2:g.132892310G= GRCh38
NC_000005.9:g.132228002G= , CM000667.1:g.132228002G= GRCh37
NC_000005.8:g.132255901G= NCBI36
NG_030340.1:g.76353C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265343.10:c.2491C= MANE Select ENSP00000265343.5:p.Arg831=
ENST00000265343.9:c.2491C= ENSP00000265343.5:p.Arg831=
ENST00000378595.7:c.2491C= ENSP00000367858.3:p.Arg831=
NM_014423.3:c.2491C= NP_055238.1:p.Arg831=
XM_005271963.3:c.2491C= XP_005272020.1:p.Arg831=
XM_005271964.3:c.1357C= XP_005272021.1:p.Arg453=
XM_006714587.2:c.2404C= XP_006714650.1:p.Arg802=
XM_005271963.5:c.2491C= XP_005272020.1:p.Arg831=
XM_005271964.4:c.1357C= XP_005272021.1:p.Arg453=
XM_006714587.4:c.2404C= XP_006714650.1:p.Arg802=
NM_014423.4:c.2491C= MANE Select NP_055238.1:p.Arg831=