Canonical Allele Identifier: CA1914338926

Gene: ARID5B

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61992032_61992034delinsCAA , CM000672.2:g.61992032_61992034delinsCAA	GRCh38
NC_000010.10:g.63751791_63751793delinsCAA , CM000672.1:g.63751791_63751793delinsCAA	GRCh37
NC_000010.9:g.63421797_63421799delinsCAA	NCBI36
NG_030027.1:g.95779_95781delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279873.12:c.503-8059_503-8057delinsCAA MANE Select	ENSP00000279873.7:n.503-8059_503-8057delinsCAA
ENST00000644638.1:c.503-8059_503-8057delinsCAA	ENSP00000494412.1:n.503-8059_503-8057delinsCAA
ENST00000681100.1:c.503-8059_503-8057delinsCAA	ENSP00000506119.1:n.503-8059_503-8057delinsCAA
ENST00000279873.11:c.503-8059_503-8057delinsCAA	ENSP00000279873.7:n.503-8059_503-8057delinsCAA
NM_032199.2:c.503-8059_503-8057delinsCAA	NP_115575.1:n.503-8059_503-8057delinsCAA
XM_011540262.1:c.502+51624_502+51626delinsCAA	XP_011538564.1:n.502+51624_502+51626delinsCAA
XM_024448230.1:c.-65-8059_-65-8057delinsCAA	XP_024303998.1:n.-65-8059_-65-8057delinsCAA
NM_032199.3:c.503-8059_503-8057delinsCAA MANE Select	NP_115575.1:n.503-8059_503-8057delinsCAA