Canonical Allele Identifier: CA71636566

Gene: RARB

Linked Data

• ClinVar Variation Id: 1178914
• ClinVar RCV Id: RCV001535298
• dbSNP Id: rs56255512
• gnomAD v2: 3-25611472-GACAC-G
• gnomAD v3: 3-25569981-GACAC-G
• gnomAD v4: 3-25569981-GACAC-G
• MyVariant Identifiers: chr3:g.25611481_25611484del (hg19) ; chr3:g.25611479_25611482del (hg19) ; chr3:g.25611473_25611476del (hg19) ; chr3:g.25569988_25569991del (hg38) ; chr3:g.25569982_25569985del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25570018_25570021del , CM000665.2:g.25570018_25570021del	GRCh38
NC_000003.11:g.25611509_25611512del , CM000665.1:g.25611509_25611512del	GRCh37
NC_000003.10:g.25586513_25586516del	NCBI36
NG_029013.1:g.146756_146759del
NG_029013.3:g.745696_745699del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383772.9:c.630+100_630+103del	ENSP00000373282.5:n.630+100_630+103del
ENST00000437042.7:c.273+100_273+103del	ENSP00000398840.2:n.273+100_273+103del
ENST00000458646.2:c.273+100_273+103del	ENSP00000391391.1:n.273+100_273+103del
ENST00000462272.6:n.554+100_554+103del
ENST00000479097.6:c.449-10528_449-10525del	ENSP00000508755.1:n.449-10528_449-10525del
ENST00000480001.6:c.609+100_609+103del	ENSP00000510647.1:n.609+100_609+103del
ENST00000685523.1:c.*445+100_*445+103del	ENSP00000508765.1:n.*445+100_*445+103del
ENST00000686715.1:c.630+100_630+103del	ENSP00000510539.1:n.630+100_630+103del
ENST00000687083.1:c.609+100_609+103del	ENSP00000509681.1:n.609+100_609+103del
ENST00000687353.1:c.630+100_630+103del	ENSP00000508588.1:n.630+100_630+103del
ENST00000687676.1:c.630+100_630+103del	ENSP00000510313.1:n.630+100_630+103del
ENST00000688892.1:c.630+100_630+103del	ENSP00000510650.1:n.630+100_630+103del
ENST00000689700.1:c.303+100_303+103del	ENSP00000510200.1:n.303+100_303+103del
ENST00000690398.1:c.*224+100_*224+103del	ENSP00000510044.1:n.*224+100_*224+103del
ENST00000691580.1:c.438+114_438+117del
ENST00000691912.1:c.609+100_609+103del	ENSP00000510520.1:n.609+100_609+103del
ENST00000693261.1:c.273+100_273+103del	ENSP00000508421.1:n.273+100_273+103del
ENST00000693580.1:c.303+100_303+103del	ENSP00000510405.1:n.303+100_303+103del
ENST00000330688.9:c.609+100_609+103del MANE Select	ENSP00000332296.4:n.609+100_609+103del
ENST00000330688.8:c.609+100_609+103del	ENSP00000332296.4:n.609+100_609+103del
ENST00000383772.8:c.630+100_630+103del	ENSP00000373282.4:n.630+100_630+103del
ENST00000437042.6:c.273+100_273+103del	ENSP00000398840.2:n.273+100_273+103del
ENST00000458646.1:c.273+100_273+103del	ENSP00000391391.1:n.273+100_273+103del
ENST00000462272.5:n.625+100_625+103del
ENST00000479097.5:n.465-10528_465-10525del
ENST00000480001.5:n.625+100_625+103del
NM_000965.4:c.609+100_609+103del	NP_000956.2:n.609+100_609+103del
NM_001290216.1:c.630+100_630+103del	NP_001277145.1:n.630+100_630+103del
NM_001290217.1:c.273+100_273+103del	NP_001277146.1:n.273+100_273+103del
NM_001290266.1:c.462+100_462+103del	NP_001277195.1:n.462+100_462+103del
NM_001290276.1:c.273+100_273+103del	NP_001277205.1:n.273+100_273+103del
NM_001290277.1:c.609+100_609+103del	NP_001277206.1:n.609+100_609+103del
NM_001290300.1:c.480+100_480+103del	NP_001277229.1:n.480+100_480+103del
NM_016152.3:c.273+100_273+103del	NP_057236.1:n.273+100_273+103del
NR_110892.1:n.918-10528_918-10525del
NR_110893.1:n.1078+100_1078+103del
NM_001290216.2:c.630+100_630+103del	NP_001277145.1:n.630+100_630+103del
NM_000965.5:c.609+100_609+103del MANE Select	NP_000956.2:n.609+100_609+103del
NM_001290216.3:c.630+100_630+103del	NP_001277145.1:n.630+100_630+103del
NM_001290217.2:c.273+100_273+103del	NP_001277146.1:n.273+100_273+103del
NM_001290266.2:c.462+100_462+103del	NP_001277195.1:n.462+100_462+103del
NM_001290276.2:c.273+100_273+103del	NP_001277205.1:n.273+100_273+103del
NM_001290300.2:c.480+100_480+103del	NP_001277229.1:n.480+100_480+103del
NM_016152.4:c.273+100_273+103del	NP_057236.1:n.273+100_273+103del
NR_110892.2:n.918-10528_918-10525del
NR_110893.2:n.1078+100_1078+103del