Canonical Allele Identifier: CA2692437277

Gene: RXRA

Linked Data

• gnomAD v4: 9-134408368-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408372del , CM000671.2:g.134408372del	GRCh38
NC_000009.11:g.137300218del , CM000671.1:g.137300218del	GRCh37
NC_000009.10:g.136440039del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.430+73del MANE Select	ENSP00000419692.1:n.430+73del
ENST00000672570.1:c.349+73del	ENSP00000500402.1:n.349+73del
ENST00000356384.4:n.840+73del
ENST00000481739.1:c.430+73del	ENSP00000419692.1:n.430+73del
NM_001291920.1:c.349+73del	NP_001278849.1:n.349+73del
NM_001291921.1:c.139+73del	NP_001278850.1:n.139+73del
NM_002957.5:c.430+73del	NP_002948.1:n.430+73del
NM_002957.6:c.430+73del MANE Select	NP_002948.1:n.430+73del
NM_001291921.2:c.139+73del	NP_001278850.1:n.139+73del
NM_001291920.2:c.349+73del	NP_001278849.1:n.349+73del