Canonical Allele Identifier: CA2648887522

Gene: RXRG

Linked Data

• gnomAD v4: 1-165419750-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419754del , CM000663.2:g.165419754del	GRCh38
NC_000001.10:g.165388991del , CM000663.1:g.165388991del	GRCh37
NC_000001.9:g.163655615del	NCBI36
NG_029517.1:g.30605del
NG_029517.2:g.30605del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.442+119del MANE Select	ENSP00000352900.5:n.442+119del
ENST00000359842.9:c.442+119del	ENSP00000352900.5:n.442+119del
ENST00000470566.1:n.367+119del
ENST00000619224.1:c.73+119del	ENSP00000482458.1:n.73+119del
NM_001256570.1:c.73+119del	NP_001243499.1:n.73+119del
NM_001256571.1:c.73+119del	NP_001243500.1:n.73+119del
NM_006917.4:c.442+119del	NP_008848.1:n.442+119del
NM_006917.5:c.442+119del MANE Select	NP_008848.1:n.442+119del
NM_001256571.2:c.73+119del	NP_001243500.1:n.73+119del
NM_001256570.2:c.73+119del	NP_001243499.1:n.73+119del