Canonical Allele Identifier: CA2675251649
Gene: AFF4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132886216_132886217del , CM000667.2:g.132886216_132886217del GRCh38
NC_000005.9:g.132221908_132221909del , CM000667.1:g.132221908_132221909del GRCh37
NC_000005.8:g.132249807_132249808del NCBI36
NG_030340.1:g.82450_82451del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265343.10:c.3099+97_3099+98del MANE Select ENSP00000265343.5:n.3099+97_3099+98del
ENST00000265343.9:c.3099+97_3099+98del ENSP00000265343.5:n.3099+97_3099+98del
NM_014423.3:c.3099+97_3099+98del NP_055238.1:n.3099+97_3099+98del
XM_005271963.3:c.3099+97_3099+98del XP_005272020.1:n.3099+97_3099+98del
XM_005271964.3:c.1965+97_1965+98del XP_005272021.1:n.1965+97_1965+98del
XM_006714587.2:c.3012+97_3012+98del XP_006714650.1:n.3012+97_3012+98del
XM_005271963.5:c.3099+97_3099+98del XP_005272020.1:n.3099+97_3099+98del
XM_005271964.4:c.1965+97_1965+98del XP_005272021.1:n.1965+97_1965+98del
XM_006714587.4:c.3012+97_3012+98del XP_006714650.1:n.3012+97_3012+98del
NM_014423.4:c.3099+97_3099+98del MANE Select NP_055238.1:n.3099+97_3099+98del