Canonical Allele Identifier: CA2788229479

Gene: ARID5B

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61963741_61963742del , CM000672.2:g.61963741_61963742del	GRCh38
NC_000010.10:g.63723500_63723501del , CM000672.1:g.63723500_63723501del	GRCh37
NC_000010.9:g.63393506_63393507del	NCBI36
NG_030027.1:g.67488_67489del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279873.12:c.502+23333_502+23334del MANE Select	ENSP00000279873.7:n.502+23333_502+23334del
ENST00000644638.1:c.502+23333_502+23334del	ENSP00000494412.1:n.502+23333_502+23334del
ENST00000681100.1:c.502+23333_502+23334del	ENSP00000506119.1:n.502+23333_502+23334del
ENST00000279873.11:c.502+23333_502+23334del	ENSP00000279873.7:n.502+23333_502+23334del
NM_032199.2:c.502+23333_502+23334del	NP_115575.1:n.502+23333_502+23334del
XM_011540262.1:c.502+23333_502+23334del	XP_011538564.1:n.502+23333_502+23334del
XM_024448230.1:c.-66+23333_-66+23334del	XP_024303998.1:n.-66+23333_-66+23334del
NM_032199.3:c.502+23333_502+23334del MANE Select	NP_115575.1:n.502+23333_502+23334del