Canonical Allele Identifier: CA3408779
Gene: AFF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132887526T>C , CM000667.2:g.132887526T>C GRCh38
NC_000005.9:g.132223218T>C , CM000667.1:g.132223218T>C GRCh37
NC_000005.8:g.132251117T>C NCBI36
NG_030340.1:g.81137A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265343.10:c.3000A>G MANE Select ENSP00000265343.5:p.Val1000=
ENST00000265343.9:c.3000A>G ENSP00000265343.5:p.Val1000=
NM_014423.3:c.3000A>G NP_055238.1:p.Val1000=
XM_005271963.3:c.3000A>G XP_005272020.1:p.Val1000=
XM_005271964.3:c.1866A>G XP_005272021.1:p.Val622=
XM_006714587.2:c.2913A>G XP_006714650.1:p.Val971=
XM_005271963.5:c.3000A>G XP_005272020.1:p.Val1000=
XM_005271964.4:c.1866A>G XP_005272021.1:p.Val622=
XM_006714587.4:c.2913A>G XP_006714650.1:p.Val971=
NM_014423.4:c.3000A>G MANE Select NP_055238.1:p.Val1000=