Canonical Allele Identifier: CA1914337262

Gene: ARID5B

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61985799_61985802delinsAAAT , CM000672.2:g.61985799_61985802delinsAAAT	GRCh38
NC_000010.10:g.63745558_63745561delinsAAAT , CM000672.1:g.63745558_63745561delinsAAAT	GRCh37
NC_000010.9:g.63415564_63415567delinsAAAT	NCBI36
NG_030027.1:g.89546_89549delinsAAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279873.12:c.503-14292_503-14289delinsAAAT MANE Select	ENSP00000279873.7:n.503-14292_503-14289delinsAAAT
ENST00000644638.1:c.503-14292_503-14289delinsAAAT	ENSP00000494412.1:n.503-14292_503-14289delinsAAAT
ENST00000681100.1:c.503-14292_503-14289delinsAAAT	ENSP00000506119.1:n.503-14292_503-14289delinsAAAT
ENST00000279873.11:c.503-14292_503-14289delinsAAAT	ENSP00000279873.7:n.503-14292_503-14289delinsAAAT
NM_032199.2:c.503-14292_503-14289delinsAAAT	NP_115575.1:n.503-14292_503-14289delinsAAAT
XM_011540262.1:c.502+45391_502+45394delinsAAAT	XP_011538564.1:n.502+45391_502+45394delinsAAAT
XM_024448230.1:c.-65-14292_-65-14289delinsAAAT	XP_024303998.1:n.-65-14292_-65-14289delinsAAAT
NM_032199.3:c.503-14292_503-14289delinsAAAT MANE Select	NP_115575.1:n.503-14292_503-14289delinsAAAT