Canonical Allele Identifier: CA2573052133

Gene: RARB

Linked Data

• ClinVar Variation Id: 1309156
• ClinVar RCV Id: RCV001765325
• dbSNP Id: rs2125325451

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25593588_25593589delinsCA , CM000665.2:g.25593588_25593589delinsCA	GRCh38
NC_000003.11:g.25635079_25635080delinsCA , CM000665.1:g.25635079_25635080delinsCA	GRCh37
NC_000003.10:g.25610083_25610084delinsCA	NCBI36
NG_029013.1:g.170326_170327delinsCA
NG_029013.3:g.769266_769267delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383772.9:c.893_894delinsCA	ENSP00000373282.5:p.His298Pro
ENST00000437042.7:c.536_537delinsCA	ENSP00000398840.2:p.His179Pro
ENST00000458646.2:c.536_537delinsCA	ENSP00000391391.1:p.His179Pro
ENST00000462272.6:n.817_818delinsCA
ENST00000479097.6:c.*261_*262delinsCA	ENSP00000508755.1:n.*261_*262delinsCA
ENST00000480001.6:c.787-932_787-931delinsCA	ENSP00000510647.1:n.787-932_787-931delinsCA
ENST00000685523.1:c.*708_*709delinsCA	ENSP00000508765.1:n.*708_*709delinsCA
ENST00000686715.1:c.893_894delinsCA	ENSP00000510539.1:p.His298Pro
ENST00000687083.1:c.787-2832_787-2831delinsCA	ENSP00000509681.1:n.787-2832_787-2831delinsCA
ENST00000687353.1:c.893_894delinsCA	ENSP00000508588.1:p.His298Pro
ENST00000687676.1:c.893_894delinsCA	ENSP00000510313.1:p.His298Pro
ENST00000688892.1:c.893_894delinsCA	ENSP00000510650.1:p.His298Pro
ENST00000689700.1:c.618_619delinsCA	ENSP00000510200.1:n.618_619delinsCA
ENST00000690398.1:c.*487_*488delinsCA	ENSP00000510044.1:n.*487_*488delinsCA
ENST00000691580.1:c.701_702delinsCA
ENST00000691912.1:c.787-53_787-52delinsCA	ENSP00000510520.1:n.787-53_787-52delinsCA
ENST00000693261.1:c.536_537delinsCA	ENSP00000508421.1:p.His179Pro
ENST00000693580.1:c.304-932_304-931delinsCA	ENSP00000510405.1:n.304-932_304-931delinsCA
ENST00000330688.9:c.872_873delinsCA MANE Select	ENSP00000332296.4:p.His291Pro
ENST00000330688.8:c.872_873delinsCA	ENSP00000332296.4:p.His291Pro
ENST00000383772.8:c.893_894delinsCA	ENSP00000373282.4:p.His298Pro
ENST00000437042.6:c.536_537delinsCA	ENSP00000398840.2:p.His179Pro
ENST00000458646.1:c.536_537delinsCA	ENSP00000391391.1:p.His179Pro
ENST00000462272.5:n.803-53_803-52delinsCA
ENST00000479097.5:n.727_728delinsCA
ENST00000480001.5:n.803-932_803-931delinsCA
NM_000965.4:c.872_873delinsCA	NP_000956.2:p.His291Pro
NM_001290216.1:c.893_894delinsCA	NP_001277145.1:p.His298Pro
NM_001290217.1:c.536_537delinsCA	NP_001277146.1:p.His179Pro
NM_001290266.1:c.725_726delinsCA	NP_001277195.1:p.His242Pro
NM_001290276.1:c.536_537delinsCA	NP_001277205.1:p.His179Pro
NM_001290277.1:c.787-53_787-52delinsCA	NP_001277206.1:n.787-53_787-52delinsCA
NM_001290300.1:c.743_744delinsCA	NP_001277229.1:p.His248Pro
NM_016152.3:c.536_537delinsCA	NP_057236.1:p.His179Pro
NR_110892.1:n.1180_1181delinsCA
NR_110893.1:n.1256-932_1256-931delinsCA
NM_001290216.2:c.893_894delinsCA	NP_001277145.1:p.His298Pro
NM_000965.5:c.872_873delinsCA MANE Select	NP_000956.2:p.His291Pro
NM_001290216.3:c.893_894delinsCA	NP_001277145.1:p.His298Pro
NM_001290217.2:c.536_537delinsCA	NP_001277146.1:p.His179Pro
NM_001290266.2:c.725_726delinsCA	NP_001277195.1:p.His242Pro
NM_001290276.2:c.536_537delinsCA	NP_001277205.1:p.His179Pro
NM_001290300.2:c.743_744delinsCA	NP_001277229.1:p.His248Pro
NM_016152.4:c.536_537delinsCA	NP_057236.1:p.His179Pro
NR_110892.2:n.1180_1181delinsCA
NR_110893.2:n.1256-932_1256-931delinsCA