Canonical Allele Identifier: CA399341222

Gene: RARA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40356120G>T , CM000679.2:g.40356120G>T	GRCh38
NC_000017.10:g.38512372G>T , CM000679.1:g.38512372G>T	GRCh37
NC_000017.9:g.35765898G>T	NCBI36
NG_027701.1:g.51950G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000964.4:c.1283G>T MANE Select	NP_000955.1:p.Gly428Val
ENST00000254066.10:c.1283G>T MANE Select	ENSP00000254066.5:p.Gly428Val
NM_000964.3:c.1283G>T	NP_000955.1:p.Gly428Val
NM_001024809.3:c.1268G>T	NP_001019980.1:p.Gly423Val
NM_001024809.4:c.1268G>T	NP_001019980.1:p.Gly423Val
NM_001145301.2:c.1283G>T	NP_001138773.1:p.Gly428Val
NM_001145301.3:c.1283G>T	NP_001138773.1:p.Gly428Val
NM_001145302.2:c.992G>T	NP_001138774.1:p.Gly331Val
NM_001145302.3:c.992G>T	NP_001138774.1:p.Gly331Val
ENST00000254066.9:c.1283G>T	ENSP00000254066.5:p.Gly428Val
ENST00000394081.7:c.1268G>T	ENSP00000377643.3:p.Gly423Val
ENST00000394086.7:c.1331G>T	ENSP00000377648.3:p.Gly444Val
ENST00000394089.6:c.1283G>T	ENSP00000377649.2:p.Gly428Val
ENST00000420042.1:n.959G>T
ENST00000425707.7:c.992G>T	ENSP00000389993.3:p.Gly331Val
XM_005257552.3:c.1331G>T	XP_005257609.1:p.Gly444Val
XM_005257552.5:c.1331G>T	XP_005257609.1:p.Gly444Val
XM_005257553.1:c.1283G>T	XP_005257610.1:p.Gly428Val
XM_005257554.1:c.1283G>T	XP_005257611.1:p.Gly428Val
XM_011525095.1:c.1283G>T	XP_011523397.1:p.Gly428Val
XM_011525096.1:c.1109G>T	XP_011523398.1:p.Gly370Val
XM_017024920.2:c.926G>T	XP_016880409.1:p.Gly309Val