Canonical Allele Identifier: CA3408894
Gene: AFF4 HGNC NCBI

Linked Data

dbSNP Id: rs780974502

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132892208_132892210del , CM000667.2:g.132892208_132892210del GRCh38
NC_000005.9:g.132227900_132227902del , CM000667.1:g.132227900_132227902del GRCh37
NC_000005.8:g.132255799_132255801del NCBI36
NG_030340.1:g.76459_76461del

Transcript Alleles

HGVS Amino-acid change
ENST00000265343.10:c.2597_2599del MANE Select ENSP00000265343.5:p.Lys866del
ENST00000265343.9:c.2597_2599del ENSP00000265343.5:p.Lys866del
ENST00000378595.7:c.2597_2599del ENSP00000367858.3:p.Lys866del
NM_014423.3:c.2597_2599del NP_055238.1:p.Lys866del
XM_005271963.3:c.2597_2599del XP_005272020.1:p.Lys866del
XM_005271964.3:c.1463_1465del XP_005272021.1:p.Lys488del
XM_006714587.2:c.2510_2512del XP_006714650.1:p.Lys837del
XM_005271963.5:c.2597_2599del XP_005272020.1:p.Lys866del
XM_005271964.4:c.1463_1465del XP_005272021.1:p.Lys488del
XM_006714587.4:c.2510_2512del XP_006714650.1:p.Lys837del
NM_014423.4:c.2597_2599del MANE Select NP_055238.1:p.Lys866del