Canonical Allele Identifier: CA1583372366
Gene: AFF4 HGNC NCBI

Linked Data

dbSNP Id: rs1760270620

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132892000del , CM000667.2:g.132892000del GRCh38
NC_000005.9:g.132227692del , CM000667.1:g.132227692del GRCh37
NC_000005.8:g.132255591del NCBI36
NG_030340.1:g.76663del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265343.10:c.2637+164del MANE Select ENSP00000265343.5:n.2637+164del
ENST00000265343.9:c.2637+164del ENSP00000265343.5:n.2637+164del
ENST00000378595.7:c.*98del ENSP00000367858.3:n.*98del
NM_014423.3:c.2637+164del NP_055238.1:n.2637+164del
XM_005271963.3:c.2637+164del XP_005272020.1:n.2637+164del
XM_005271964.3:c.1503+164del XP_005272021.1:n.1503+164del
XM_006714587.2:c.2550+164del XP_006714650.1:n.2550+164del
XM_005271963.5:c.2637+164del XP_005272020.1:n.2637+164del
XM_005271964.4:c.1503+164del XP_005272021.1:n.1503+164del
XM_006714587.4:c.2550+164del XP_006714650.1:n.2550+164del
NM_014423.4:c.2637+164del MANE Select NP_055238.1:n.2637+164del