Canonical Allele Identifier: CA5317726

Gene: RXRA

Linked Data

• dbSNP Id: rs775970676
• ExAC: 9:137300129 C / T
• gnomAD v2: 9-137300129-C-T
• gnomAD v3: 9-134408283-C-T
• gnomAD v4: 9-134408283-C-T
• MyVariant Identifiers: chr9:g.137300129C>T (hg19) ; chr9:g.134408283C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408283C>T , CM000671.2:g.134408283C>T	GRCh38
NC_000009.11:g.137300129C>T , CM000671.1:g.137300129C>T	GRCh37
NC_000009.10:g.136439950C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.414C>T MANE Select	ENSP00000419692.1:p.Cys138=
ENST00000672570.1:c.333C>T	ENSP00000500402.1:p.Cys111=
ENST00000356384.4:n.824C>T
ENST00000481739.1:c.414C>T	ENSP00000419692.1:p.Cys138=
NM_001291920.1:c.333C>T	NP_001278849.1:p.Cys111=
NM_001291921.1:c.123C>T	NP_001278850.1:p.Cys41=
NM_002957.5:c.414C>T	NP_002948.1:p.Cys138=
NM_002957.6:c.414C>T MANE Select	NP_002948.1:p.Cys138=
NM_001291921.2:c.123C>T	NP_001278850.1:p.Cys41=
NM_001291920.2:c.333C>T	NP_001278849.1:p.Cys111=