Canonical Allele Identifier: CA2675252556

Gene: AFF4

Linked Data

• gnomAD v4: 5-132892049-A-AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132892049_132892050insGT , CM000667.2:g.132892049_132892050insGT	GRCh38
NC_000005.9:g.132227741_132227742insGT , CM000667.1:g.132227741_132227742insGT	GRCh37
NC_000005.8:g.132255640_132255641insGT	NCBI36
NG_030340.1:g.76613_76614insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265343.10:c.2637+114_2637+115insAC MANE Select	ENSP00000265343.5:n.2637+114_2637+115insAC
ENST00000265343.9:c.2637+114_2637+115insAC	ENSP00000265343.5:n.2637+114_2637+115insAC
ENST00000378595.7:c.*48_*49insAC	ENSP00000367858.3:n.*48_*49insAC
NM_014423.3:c.2637+114_2637+115insAC	NP_055238.1:n.2637+114_2637+115insAC
XM_005271963.3:c.2637+114_2637+115insAC	XP_005272020.1:n.2637+114_2637+115insAC
XM_005271964.3:c.1503+114_1503+115insAC	XP_005272021.1:n.1503+114_1503+115insAC
XM_006714587.2:c.2550+114_2550+115insAC	XP_006714650.1:n.2550+114_2550+115insAC
XM_005271963.5:c.2637+114_2637+115insAC	XP_005272020.1:n.2637+114_2637+115insAC
XM_005271964.4:c.1503+114_1503+115insAC	XP_005272021.1:n.1503+114_1503+115insAC
XM_006714587.4:c.2550+114_2550+115insAC	XP_006714650.1:n.2550+114_2550+115insAC
NM_014423.4:c.2637+114_2637+115insAC MANE Select	NP_055238.1:n.2637+114_2637+115insAC