Canonical Allele Identifier: CA1147157619

Gene: RXRG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419397_165419408delinsTTTTTTTTTTTT , CM000663.2:g.165419397_165419408delinsTTTTTTTTTTTT	GRCh38
NC_000001.10:g.165388634_165388645delinsTTTTTTTTTTTT , CM000663.1:g.165388634_165388645delinsTTTTTTTTTTTT	GRCh37
NC_000001.9:g.163655258_163655269delinsTTTTTTTTTTTT	NCBI36
NG_029517.1:g.30948_30959delinsAAAAAAAAAAAA
NG_029517.2:g.30948_30959delinsAAAAAAAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.442+462_442+473delinsAAAAAAAAAAAA MANE Select	ENSP00000352900.5:n.442+462_442+473delinsAAAAAAAAAAAA
ENST00000359842.9:c.442+462_442+473delinsAAAAAAAAAAAA	ENSP00000352900.5:n.442+462_442+473delinsAAAAAAAAAAAA
ENST00000470566.1:n.367+462_367+473delinsAAAAAAAAAAAA
ENST00000619224.1:c.73+462_73+473delinsAAAAAAAAAAAA	ENSP00000482458.1:n.73+462_73+473delinsAAAAAAAAAAAA
NM_001256570.1:c.73+462_73+473delinsAAAAAAAAAAAA	NP_001243499.1:n.73+462_73+473delinsAAAAAAAAAAAA
NM_001256571.1:c.73+462_73+473delinsAAAAAAAAAAAA	NP_001243500.1:n.73+462_73+473delinsAAAAAAAAAAAA
NM_006917.4:c.442+462_442+473delinsAAAAAAAAAAAA	NP_008848.1:n.442+462_442+473delinsAAAAAAAAAAAA
NM_006917.5:c.442+462_442+473delinsAAAAAAAAAAAA MANE Select	NP_008848.1:n.442+462_442+473delinsAAAAAAAAAAAA
NM_001256571.2:c.73+462_73+473delinsAAAAAAAAAAAA	NP_001243500.1:n.73+462_73+473delinsAAAAAAAAAAAA
NM_001256570.2:c.73+462_73+473delinsAAAAAAAAAAAA	NP_001243499.1:n.73+462_73+473delinsAAAAAAAAAAAA