Canonical Allele Identifier: CA2710360003

Gene: AFF4

Linked Data

• dbSNP Id: rs2150069448

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132892093_132892094del , CM000667.2:g.132892093_132892094del	GRCh38
NC_000005.9:g.132227785_132227786del , CM000667.1:g.132227785_132227786del	GRCh37
NC_000005.8:g.132255684_132255685del	NCBI36
NG_030340.1:g.76571_76572del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265343.10:c.2637+72_2637+73del MANE Select	ENSP00000265343.5:n.2637+72_2637+73del
ENST00000265343.9:c.2637+72_2637+73del	ENSP00000265343.5:n.2637+72_2637+73del
ENST00000378595.7:c.*6_*7del	ENSP00000367858.3:n.*6_*7del
NM_014423.3:c.2637+72_2637+73del	NP_055238.1:n.2637+72_2637+73del
XM_005271963.3:c.2637+72_2637+73del	XP_005272020.1:n.2637+72_2637+73del
XM_005271964.3:c.1503+72_1503+73del	XP_005272021.1:n.1503+72_1503+73del
XM_006714587.2:c.2550+72_2550+73del	XP_006714650.1:n.2550+72_2550+73del
XM_005271963.5:c.2637+72_2637+73del	XP_005272020.1:n.2637+72_2637+73del
XM_005271964.4:c.1503+72_1503+73del	XP_005272021.1:n.1503+72_1503+73del
XM_006714587.4:c.2550+72_2550+73del	XP_006714650.1:n.2550+72_2550+73del
NM_014423.4:c.2637+72_2637+73del MANE Select	NP_055238.1:n.2637+72_2637+73del