Canonical Allele Identifier: CA1583372375

Gene: AFF4

Linked Data

• dbSNP Id: rs1760270919

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132892012_132892016del , CM000667.2:g.132892012_132892016del	GRCh38
NC_000005.9:g.132227704_132227708del , CM000667.1:g.132227704_132227708del	GRCh37
NC_000005.8:g.132255603_132255607del	NCBI36
NG_030340.1:g.76649_76653del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265343.10:c.2637+150_2637+154del MANE Select	ENSP00000265343.5:n.2637+150_2637+154del
ENST00000265343.9:c.2637+150_2637+154del	ENSP00000265343.5:n.2637+150_2637+154del
ENST00000378595.7:c.*84_*88del	ENSP00000367858.3:n.*84_*88del
NM_014423.3:c.2637+150_2637+154del	NP_055238.1:n.2637+150_2637+154del
XM_005271963.3:c.2637+150_2637+154del	XP_005272020.1:n.2637+150_2637+154del
XM_005271964.3:c.1503+150_1503+154del	XP_005272021.1:n.1503+150_1503+154del
XM_006714587.2:c.2550+150_2550+154del	XP_006714650.1:n.2550+150_2550+154del
XM_005271963.5:c.2637+150_2637+154del	XP_005272020.1:n.2637+150_2637+154del
XM_005271964.4:c.1503+150_1503+154del	XP_005272021.1:n.1503+150_1503+154del
XM_006714587.4:c.2550+150_2550+154del	XP_006714650.1:n.2550+150_2550+154del
NM_014423.4:c.2637+150_2637+154del MANE Select	NP_055238.1:n.2637+150_2637+154del