Canonical Allele Identifier: CA1914327450

Gene: ARID5B

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61963677_61963679delinsCAT , CM000672.2:g.61963677_61963679delinsCAT	GRCh38
NC_000010.10:g.63723436_63723438delinsCAT , CM000672.1:g.63723436_63723438delinsCAT	GRCh37
NC_000010.9:g.63393442_63393444delinsCAT	NCBI36
NG_030027.1:g.67424_67426delinsCAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000279873.12:c.502+23269_502+23271delinsCAT MANE Select	ENSP00000279873.7:n.502+23269_502+23271delinsCAT
ENST00000644638.1:c.502+23269_502+23271delinsCAT	ENSP00000494412.1:n.502+23269_502+23271delinsCAT
ENST00000681100.1:c.502+23269_502+23271delinsCAT	ENSP00000506119.1:n.502+23269_502+23271delinsCAT
ENST00000279873.11:c.502+23269_502+23271delinsCAT	ENSP00000279873.7:n.502+23269_502+23271delinsCAT
NM_032199.2:c.502+23269_502+23271delinsCAT	NP_115575.1:n.502+23269_502+23271delinsCAT
XM_011540262.1:c.502+23269_502+23271delinsCAT	XP_011538564.1:n.502+23269_502+23271delinsCAT
XM_024448230.1:c.-66+23269_-66+23271delinsCAT	XP_024303998.1:n.-66+23269_-66+23271delinsCAT
NM_032199.3:c.502+23269_502+23271delinsCAT MANE Select	NP_115575.1:n.502+23269_502+23271delinsCAT