Canonical Allele Identifier: CA1583372364

Gene: AFF4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132891999_132892000delinsAT , CM000667.2:g.132891999_132892000delinsAT	GRCh38
NC_000005.9:g.132227691_132227692delinsAT , CM000667.1:g.132227691_132227692delinsAT	GRCh37
NC_000005.8:g.132255590_132255591delinsAT	NCBI36
NG_030340.1:g.76663_76664delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265343.10:c.2637+164_2637+165delinsAT MANE Select	ENSP00000265343.5:n.2637+164_2637+165delinsAT
ENST00000265343.9:c.2637+164_2637+165delinsAT	ENSP00000265343.5:n.2637+164_2637+165delinsAT
ENST00000378595.7:c.*98_*99delinsAT	ENSP00000367858.3:n.*98_*99delinsAT
NM_014423.3:c.2637+164_2637+165delinsAT	NP_055238.1:n.2637+164_2637+165delinsAT
XM_005271963.3:c.2637+164_2637+165delinsAT	XP_005272020.1:n.2637+164_2637+165delinsAT
XM_005271964.3:c.1503+164_1503+165delinsAT	XP_005272021.1:n.1503+164_1503+165delinsAT
XM_006714587.2:c.2550+164_2550+165delinsAT	XP_006714650.1:n.2550+164_2550+165delinsAT
XM_005271963.5:c.2637+164_2637+165delinsAT	XP_005272020.1:n.2637+164_2637+165delinsAT
XM_005271964.4:c.1503+164_1503+165delinsAT	XP_005272021.1:n.1503+164_1503+165delinsAT
XM_006714587.4:c.2550+164_2550+165delinsAT	XP_006714650.1:n.2550+164_2550+165delinsAT
NM_014423.4:c.2637+164_2637+165delinsAT MANE Select	NP_055238.1:n.2637+164_2637+165delinsAT