Canonical Allele Identifier: CA1914327437

Gene: ARID5B

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61963659_61963661delinsGCT , CM000672.2:g.61963659_61963661delinsGCT	GRCh38
NC_000010.10:g.63723418_63723420delinsGCT , CM000672.1:g.63723418_63723420delinsGCT	GRCh37
NC_000010.9:g.63393424_63393426delinsGCT	NCBI36
NG_030027.1:g.67406_67408delinsGCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000279873.12:c.502+23251_502+23253delinsGCT MANE Select	ENSP00000279873.7:n.502+23251_502+23253delinsGCT
ENST00000644638.1:c.502+23251_502+23253delinsGCT	ENSP00000494412.1:n.502+23251_502+23253delinsGCT
ENST00000681100.1:c.502+23251_502+23253delinsGCT	ENSP00000506119.1:n.502+23251_502+23253delinsGCT
ENST00000279873.11:c.502+23251_502+23253delinsGCT	ENSP00000279873.7:n.502+23251_502+23253delinsGCT
NM_032199.2:c.502+23251_502+23253delinsGCT	NP_115575.1:n.502+23251_502+23253delinsGCT
XM_011540262.1:c.502+23251_502+23253delinsGCT	XP_011538564.1:n.502+23251_502+23253delinsGCT
XM_024448230.1:c.-66+23251_-66+23253delinsGCT	XP_024303998.1:n.-66+23251_-66+23253delinsGCT
NM_032199.3:c.502+23251_502+23253delinsGCT MANE Select	NP_115575.1:n.502+23251_502+23253delinsGCT