Canonical Allele Identifier: CA351889053

Gene: RARB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25596420G>A , CM000665.2:g.25596420G>A	GRCh38
NC_000003.11:g.25637911G>A , CM000665.1:g.25637911G>A	GRCh37
NC_000003.10:g.25612915G>A	NCBI36
NG_029013.1:g.173158G>A
NG_029013.3:g.772098G>A
NG_052961.1:g.72953C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000965.5:c.1151G>A MANE Select	NP_000956.2:p.Gly384Asp
ENST00000330688.9:c.1151G>A MANE Select	ENSP00000332296.4:p.Gly384Asp
NM_000965.4:c.1151G>A	NP_000956.2:p.Gly384Asp
NM_001290216.1:c.1172G>A	NP_001277145.1:p.Gly391Asp
NM_001290216.2:c.1172G>A	NP_001277145.1:p.Gly391Asp
NM_001290216.3:c.1172G>A	NP_001277145.1:p.Gly391Asp
NM_001290217.1:c.815G>A	NP_001277146.1:p.Gly272Asp
NM_001290217.2:c.815G>A	NP_001277146.1:p.Gly272Asp
NM_001290266.1:c.1004G>A	NP_001277195.1:p.Gly335Asp
NM_001290266.2:c.1004G>A	NP_001277195.1:p.Gly335Asp
NM_001290276.1:c.815G>A	NP_001277205.1:p.Gly272Asp
NM_001290276.2:c.815G>A	NP_001277205.1:p.Gly272Asp
NM_001290277.1:c.1013G>A	NP_001277206.1:p.Gly338Asp
NM_001290300.1:c.1022G>A	NP_001277229.1:p.Gly341Asp
NM_001290300.2:c.1022G>A	NP_001277229.1:p.Gly341Asp
NM_016152.3:c.815G>A	NP_057236.1:p.Gly272Asp
NM_016152.4:c.815G>A	NP_057236.1:p.Gly272Asp
NR_110892.1:n.1459G>A
NR_110892.2:n.1459G>A
NR_110893.1:n.1415G>A
NR_110893.2:n.1415G>A
ENST00000330688.8:c.1151G>A	ENSP00000332296.4:p.Gly384Asp
ENST00000383772.8:c.1172G>A	ENSP00000373282.4:p.Gly391Asp
ENST00000383772.9:c.1172G>A	ENSP00000373282.5:p.Gly391Asp
ENST00000437042.6:c.815G>A	ENSP00000398840.2:p.Gly272Asp
ENST00000437042.7:c.815G>A	ENSP00000398840.2:p.Gly272Asp
ENST00000458646.1:c.815G>A	ENSP00000391391.1:p.Gly272Asp
ENST00000458646.2:c.815G>A	ENSP00000391391.1:p.Gly272Asp
ENST00000462272.5:n.1029G>A
ENST00000462272.6:n.1096G>A
ENST00000479097.5:n.1006G>A
ENST00000479097.6:c.*540G>A	ENSP00000508755.1:n.*540G>A
ENST00000480001.5:n.962G>A
ENST00000480001.6:c.*127G>A	ENSP00000510647.1:n.*127G>A
ENST00000685523.1:c.*987G>A	ENSP00000508765.1:n.*987G>A
ENST00000686715.1:c.1172G>A	ENSP00000510539.1:p.Gly391Asp
ENST00000687083.1:c.787G>A	ENSP00000509681.1:p.Val263Met
ENST00000687353.1:c.1172G>A	ENSP00000508588.1:p.Gly391Asp
ENST00000687676.1:c.1172G>A	ENSP00000510313.1:p.Gly391Asp
ENST00000688892.1:c.1172G>A	ENSP00000510650.1:p.Gly391Asp
ENST00000689700.1:c.897G>A	ENSP00000510200.1:n.897G>A
ENST00000690398.1:c.*766G>A	ENSP00000510044.1:n.*766G>A
ENST00000691580.1:c.980G>A
ENST00000691912.1:c.1013G>A	ENSP00000510520.1:p.Gly338Asp
ENST00000693261.1:c.815G>A	ENSP00000508421.1:p.Gly272Asp
ENST00000693580.1:c.463G>A	ENSP00000510405.1:n.463G>A