Canonical Allele Identifier: CA1883176829

Gene: RXRA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408312_134408313delinsTG , CM000671.2:g.134408312_134408313delinsTG	GRCh38
NC_000009.11:g.137300158_137300159delinsTG , CM000671.1:g.137300158_137300159delinsTG	GRCh37
NC_000009.10:g.136439979_136439980delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.430+13_430+14delinsTG MANE Select	ENSP00000419692.1:n.430+13_430+14delinsTG
ENST00000672570.1:c.349+13_349+14delinsTG	ENSP00000500402.1:n.349+13_349+14delinsTG
ENST00000356384.4:n.840+13_840+14delinsTG
ENST00000481739.1:c.430+13_430+14delinsTG	ENSP00000419692.1:n.430+13_430+14delinsTG
NM_001291920.1:c.349+13_349+14delinsTG	NP_001278849.1:n.349+13_349+14delinsTG
NM_001291921.1:c.139+13_139+14delinsTG	NP_001278850.1:n.139+13_139+14delinsTG
NM_002957.5:c.430+13_430+14delinsTG	NP_002948.1:n.430+13_430+14delinsTG
NM_002957.6:c.430+13_430+14delinsTG MANE Select	NP_002948.1:n.430+13_430+14delinsTG
NM_001291921.2:c.139+13_139+14delinsTG	NP_001278850.1:n.139+13_139+14delinsTG
NM_001291920.2:c.349+13_349+14delinsTG	NP_001278849.1:n.349+13_349+14delinsTG