Canonical Allele Identifier: CA375452690

Gene: RXRA

Linked Data

• gnomAD v4: 9-134408282-G-T
• MyVariant Identifiers: chr9:g.137300128G>T (hg19) ; chr9:g.134408282G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408282G>T , CM000671.2:g.134408282G>T	GRCh38
NC_000009.11:g.137300128G>T , CM000671.1:g.137300128G>T	GRCh37
NC_000009.10:g.136439949G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.413G>T MANE Select	ENSP00000419692.1:p.Cys138Phe
ENST00000672570.1:c.332G>T	ENSP00000500402.1:p.Cys111Phe
ENST00000356384.4:n.823G>T
ENST00000481739.1:c.413G>T	ENSP00000419692.1:p.Cys138Phe
NM_001291920.1:c.332G>T	NP_001278849.1:p.Cys111Phe
NM_001291921.1:c.122G>T	NP_001278850.1:p.Cys41Phe
NM_002957.5:c.413G>T	NP_002948.1:p.Cys138Phe
NM_002957.6:c.413G>T MANE Select	NP_002948.1:p.Cys138Phe
NM_001291921.2:c.122G>T	NP_001278850.1:p.Cys41Phe
NM_001291920.2:c.332G>T	NP_001278849.1:p.Cys111Phe