Canonical Allele Identifier: CA1914325290

Gene: ARID5B

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61958660_61958662delinsCTT , CM000672.2:g.61958660_61958662delinsCTT	GRCh38
NC_000010.10:g.63718419_63718421delinsCTT , CM000672.1:g.63718419_63718421delinsCTT	GRCh37
NC_000010.9:g.63388425_63388427delinsCTT	NCBI36
NG_030027.1:g.62407_62409delinsCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000279873.12:c.502+18252_502+18254delinsCTT MANE Select	ENSP00000279873.7:n.502+18252_502+18254delinsCTT
ENST00000644638.1:c.502+18252_502+18254delinsCTT	ENSP00000494412.1:n.502+18252_502+18254delinsCTT
ENST00000681100.1:c.502+18252_502+18254delinsCTT	ENSP00000506119.1:n.502+18252_502+18254delinsCTT
ENST00000279873.11:c.502+18252_502+18254delinsCTT	ENSP00000279873.7:n.502+18252_502+18254delinsCTT
NM_032199.2:c.502+18252_502+18254delinsCTT	NP_115575.1:n.502+18252_502+18254delinsCTT
XM_011540262.1:c.502+18252_502+18254delinsCTT	XP_011538564.1:n.502+18252_502+18254delinsCTT
XM_024448230.1:c.-66+18252_-66+18254delinsCTT	XP_024303998.1:n.-66+18252_-66+18254delinsCTT
NM_032199.3:c.502+18252_502+18254delinsCTT MANE Select	NP_115575.1:n.502+18252_502+18254delinsCTT