Canonical Allele Identifier: CA1914327426

Gene: ARID5B

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61963631_61963634delinsCTTT , CM000672.2:g.61963631_61963634delinsCTTT	GRCh38
NC_000010.10:g.63723390_63723393delinsCTTT , CM000672.1:g.63723390_63723393delinsCTTT	GRCh37
NC_000010.9:g.63393396_63393399delinsCTTT	NCBI36
NG_030027.1:g.67378_67381delinsCTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000279873.12:c.502+23223_502+23226delinsCTTT MANE Select	ENSP00000279873.7:n.502+23223_502+23226delinsCTTT
ENST00000644638.1:c.502+23223_502+23226delinsCTTT	ENSP00000494412.1:n.502+23223_502+23226delinsCTTT
ENST00000681100.1:c.502+23223_502+23226delinsCTTT	ENSP00000506119.1:n.502+23223_502+23226delinsCTTT
ENST00000279873.11:c.502+23223_502+23226delinsCTTT	ENSP00000279873.7:n.502+23223_502+23226delinsCTTT
NM_032199.2:c.502+23223_502+23226delinsCTTT	NP_115575.1:n.502+23223_502+23226delinsCTTT
XM_011540262.1:c.502+23223_502+23226delinsCTTT	XP_011538564.1:n.502+23223_502+23226delinsCTTT
XM_024448230.1:c.-66+23223_-66+23226delinsCTTT	XP_024303998.1:n.-66+23223_-66+23226delinsCTTT
NM_032199.3:c.502+23223_502+23226delinsCTTT MANE Select	NP_115575.1:n.502+23223_502+23226delinsCTTT