Canonical Allele Identifier: CA2675252559

Gene: AFF4

Linked Data

• gnomAD v4: 5-132892054-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132892055_132892056del , CM000667.2:g.132892055_132892056del	GRCh38
NC_000005.9:g.132227747_132227748del , CM000667.1:g.132227747_132227748del	GRCh37
NC_000005.8:g.132255646_132255647del	NCBI36
NG_030340.1:g.76607_76608del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265343.10:c.2637+108_2637+109del MANE Select	ENSP00000265343.5:n.2637+108_2637+109del
ENST00000265343.9:c.2637+108_2637+109del	ENSP00000265343.5:n.2637+108_2637+109del
ENST00000378595.7:c.*42_*43del	ENSP00000367858.3:n.*42_*43del
NM_014423.3:c.2637+108_2637+109del	NP_055238.1:n.2637+108_2637+109del
XM_005271963.3:c.2637+108_2637+109del	XP_005272020.1:n.2637+108_2637+109del
XM_005271964.3:c.1503+108_1503+109del	XP_005272021.1:n.1503+108_1503+109del
XM_006714587.2:c.2550+108_2550+109del	XP_006714650.1:n.2550+108_2550+109del
XM_005271963.5:c.2637+108_2637+109del	XP_005272020.1:n.2637+108_2637+109del
XM_005271964.4:c.1503+108_1503+109del	XP_005272021.1:n.1503+108_1503+109del
XM_006714587.4:c.2550+108_2550+109del	XP_006714650.1:n.2550+108_2550+109del
NM_014423.4:c.2637+108_2637+109del MANE Select	NP_055238.1:n.2637+108_2637+109del