Canonical Allele Identifier: CA375452677

Gene: RXRA

Linked Data

• MyVariant Identifiers: chr9:g.137300125T>C (hg19) ; chr9:g.134408279T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408279T>C , CM000671.2:g.134408279T>C	GRCh38
NC_000009.11:g.137300125T>C , CM000671.1:g.137300125T>C	GRCh37
NC_000009.10:g.136439946T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.410T>C MANE Select	ENSP00000419692.1:p.Ile137Thr
ENST00000672570.1:c.329T>C	ENSP00000500402.1:p.Ile110Thr
ENST00000356384.4:n.820T>C
ENST00000481739.1:c.410T>C	ENSP00000419692.1:p.Ile137Thr
NM_001291920.1:c.329T>C	NP_001278849.1:p.Ile110Thr
NM_001291921.1:c.119T>C	NP_001278850.1:p.Ile40Thr
NM_002957.5:c.410T>C	NP_002948.1:p.Ile137Thr
NM_002957.6:c.410T>C MANE Select	NP_002948.1:p.Ile137Thr
NM_001291921.2:c.119T>C	NP_001278850.1:p.Ile40Thr
NM_001291920.2:c.329T>C	NP_001278849.1:p.Ile110Thr