Canonical Allele Identifier: CA1583368811
Gene: AFF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132886270T= , CM000667.2:g.132886270T= GRCh38
NC_000005.9:g.132221962T= , CM000667.1:g.132221962T= GRCh37
NC_000005.8:g.132249861T= NCBI36
NG_030340.1:g.82393A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265343.10:c.3099+40A= MANE Select ENSP00000265343.5:n.3099+40A=
ENST00000265343.9:c.3099+40A= ENSP00000265343.5:n.3099+40A=
NM_014423.3:c.3099+40A= NP_055238.1:n.3099+40A=
XM_005271963.3:c.3099+40A= XP_005272020.1:n.3099+40A=
XM_005271964.3:c.1965+40A= XP_005272021.1:n.1965+40A=
XM_006714587.2:c.3012+40A= XP_006714650.1:n.3012+40A=
XM_005271963.5:c.3099+40A= XP_005272020.1:n.3099+40A=
XM_005271964.4:c.1965+40A= XP_005272021.1:n.1965+40A=
XM_006714587.4:c.3012+40A= XP_006714650.1:n.3012+40A=
NM_014423.4:c.3099+40A= MANE Select NP_055238.1:n.3099+40A=