Canonical Allele Identifier: CA2565916471

Gene: ARID5B

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61988010_61988011insCTATATTAATTCC , CM000672.2:g.61988010_61988011insCTATATTAATTCC	GRCh38
NC_000010.10:g.63747769_63747770insCTATATTAATTCC , CM000672.1:g.63747769_63747770insCTATATTAATTCC	GRCh37
NC_000010.9:g.63417775_63417776insCTATATTAATTCC	NCBI36
NG_030027.1:g.91757_91758insCTATATTAATTCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000279873.12:c.503-12081_503-12080insCTATATTAATTCC MANE Select	ENSP00000279873.7:n.503-12081_503-12080insCTATATTAATTCC
ENST00000644638.1:c.503-12081_503-12080insCTATATTAATTCC	ENSP00000494412.1:n.503-12081_503-12080insCTATATTAATTCC
ENST00000681100.1:c.503-12081_503-12080insCTATATTAATTCC	ENSP00000506119.1:n.503-12081_503-12080insCTATATTAATTCC
ENST00000279873.11:c.503-12081_503-12080insCTATATTAATTCC	ENSP00000279873.7:n.503-12081_503-12080insCTATATTAATTCC
NM_032199.2:c.503-12081_503-12080insCTATATTAATTCC	NP_115575.1:n.503-12081_503-12080insCTATATTAATTCC
XM_011540262.1:c.502+47602_502+47603insCTATATTAATTCC	XP_011538564.1:n.502+47602_502+47603insCTATATTAATTCC
XM_024448230.1:c.-65-12081_-65-12080insCTATATTAATTCC	XP_024303998.1:n.-65-12081_-65-12080insCTATATTAATTCC
NM_032199.3:c.503-12081_503-12080insCTATATTAATTCC MANE Select	NP_115575.1:n.503-12081_503-12080insCTATATTAATTCC