Canonical Allele Identifier: CA1583372440

Gene: AFF4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132892136_132892137delinsCA , CM000667.2:g.132892136_132892137delinsCA	GRCh38
NC_000005.9:g.132227828_132227829delinsCA , CM000667.1:g.132227828_132227829delinsCA	GRCh37
NC_000005.8:g.132255727_132255728delinsCA	NCBI36
NG_030340.1:g.76526_76527delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265343.10:c.2637+27_2637+28delinsTG MANE Select	ENSP00000265343.5:n.2637+27_2637+28delinsTG
ENST00000265343.9:c.2637+27_2637+28delinsTG	ENSP00000265343.5:n.2637+27_2637+28delinsTG
ENST00000378595.7:c.2664_2665delinsTG	ENSP00000367858.3:p.Phe888=
NM_014423.3:c.2637+27_2637+28delinsTG	NP_055238.1:n.2637+27_2637+28delinsTG
XM_005271963.3:c.2637+27_2637+28delinsTG	XP_005272020.1:n.2637+27_2637+28delinsTG
XM_005271964.3:c.1503+27_1503+28delinsTG	XP_005272021.1:n.1503+27_1503+28delinsTG
XM_006714587.2:c.2550+27_2550+28delinsTG	XP_006714650.1:n.2550+27_2550+28delinsTG
XM_005271963.5:c.2637+27_2637+28delinsTG	XP_005272020.1:n.2637+27_2637+28delinsTG
XM_005271964.4:c.1503+27_1503+28delinsTG	XP_005272021.1:n.1503+27_1503+28delinsTG
XM_006714587.4:c.2550+27_2550+28delinsTG	XP_006714650.1:n.2550+27_2550+28delinsTG
NM_014423.4:c.2637+27_2637+28delinsTG MANE Select	NP_055238.1:n.2637+27_2637+28delinsTG