Canonical Allele Identifier: CA1914327288

Gene: ARID5B

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61963326_61963327delinsTA , CM000672.2:g.61963326_61963327delinsTA	GRCh38
NC_000010.10:g.63723085_63723086delinsTA , CM000672.1:g.63723085_63723086delinsTA	GRCh37
NC_000010.9:g.63393091_63393092delinsTA	NCBI36
NG_030027.1:g.67073_67074delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279873.12:c.502+22918_502+22919delinsTA MANE Select	ENSP00000279873.7:n.502+22918_502+22919delinsTA
ENST00000644638.1:c.502+22918_502+22919delinsTA	ENSP00000494412.1:n.502+22918_502+22919delinsTA
ENST00000681100.1:c.502+22918_502+22919delinsTA	ENSP00000506119.1:n.502+22918_502+22919delinsTA
ENST00000279873.11:c.502+22918_502+22919delinsTA	ENSP00000279873.7:n.502+22918_502+22919delinsTA
NM_032199.2:c.502+22918_502+22919delinsTA	NP_115575.1:n.502+22918_502+22919delinsTA
XM_011540262.1:c.502+22918_502+22919delinsTA	XP_011538564.1:n.502+22918_502+22919delinsTA
XM_024448230.1:c.-66+22918_-66+22919delinsTA	XP_024303998.1:n.-66+22918_-66+22919delinsTA
NM_032199.3:c.502+22918_502+22919delinsTA MANE Select	NP_115575.1:n.502+22918_502+22919delinsTA