Canonical Allele Identifier: CA1914339048

Gene: ARID5B

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61992194_61992195delinsCT , CM000672.2:g.61992194_61992195delinsCT	GRCh38
NC_000010.10:g.63751953_63751954delinsCT , CM000672.1:g.63751953_63751954delinsCT	GRCh37
NC_000010.9:g.63421959_63421960delinsCT	NCBI36
NG_030027.1:g.95941_95942delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279873.12:c.503-7897_503-7896delinsCT MANE Select	ENSP00000279873.7:n.503-7897_503-7896delinsCT
ENST00000644638.1:c.503-7897_503-7896delinsCT	ENSP00000494412.1:n.503-7897_503-7896delinsCT
ENST00000681100.1:c.503-7897_503-7896delinsCT	ENSP00000506119.1:n.503-7897_503-7896delinsCT
ENST00000279873.11:c.503-7897_503-7896delinsCT	ENSP00000279873.7:n.503-7897_503-7896delinsCT
NM_032199.2:c.503-7897_503-7896delinsCT	NP_115575.1:n.503-7897_503-7896delinsCT
XM_011540262.1:c.502+51786_502+51787delinsCT	XP_011538564.1:n.502+51786_502+51787delinsCT
XM_024448230.1:c.-65-7897_-65-7896delinsCT	XP_024303998.1:n.-65-7897_-65-7896delinsCT
NM_032199.3:c.503-7897_503-7896delinsCT MANE Select	NP_115575.1:n.503-7897_503-7896delinsCT