Canonical Allele Identifier: CA446499183
Gene: AFF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132896509C>T , CM000667.2:g.132896509C>T GRCh38
NC_000005.9:g.132232201C>T , CM000667.1:g.132232201C>T GRCh37
NC_000005.8:g.132260100C>T NCBI36
NG_030340.1:g.72154G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265343.10:c.2121G>A MANE Select ENSP00000265343.5:p.Glu707=
ENST00000265343.9:c.2121G>A ENSP00000265343.5:p.Glu707=
ENST00000378595.7:c.2121G>A ENSP00000367858.3:p.Glu707=
NM_014423.3:c.2121G>A NP_055238.1:p.Glu707=
XM_005271963.3:c.2121G>A XP_005272020.1:p.Glu707=
XM_005271964.3:c.987G>A XP_005272021.1:p.Glu329=
XM_006714587.2:c.2034G>A XP_006714650.1:p.Glu678=
XM_005271963.5:c.2121G>A XP_005272020.1:p.Glu707=
XM_005271964.4:c.987G>A XP_005272021.1:p.Glu329=
XM_006714587.4:c.2034G>A XP_006714650.1:p.Glu678=
NM_014423.4:c.2121G>A MANE Select NP_055238.1:p.Glu707=