Canonical Allele Identifier: CA199763

Gene: RARA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40354320C>T , CM000679.2:g.40354320C>T	GRCh38
NC_000017.10:g.38510572C>T , CM000679.1:g.38510572C>T	GRCh37
NC_000017.9:g.35764098C>T	NCBI36
NG_027701.1:g.50150C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000964.4:c.826C>T MANE Select	NP_000955.1:p.Arg276Trp
ENST00000254066.10:c.826C>T MANE Select	ENSP00000254066.5:p.Arg276Trp
NM_000964.3:c.826C>T	NP_000955.1:p.Arg276Trp
NM_001024809.3:c.811C>T	NP_001019980.1:p.Arg271Trp
NM_001024809.4:c.811C>T	NP_001019980.1:p.Arg271Trp
NM_001145301.2:c.826C>T	NP_001138773.1:p.Arg276Trp
NM_001145301.3:c.826C>T	NP_001138773.1:p.Arg276Trp
NM_001145302.2:c.535C>T	NP_001138774.1:p.Arg179Trp
NM_001145302.3:c.535C>T	NP_001138774.1:p.Arg179Trp
ENST00000254066.9:c.826C>T	ENSP00000254066.5:p.Arg276Trp
ENST00000394081.7:c.811C>T	ENSP00000377643.3:p.Arg271Trp
ENST00000394086.7:c.874C>T	ENSP00000377648.3:p.Arg292Trp
ENST00000394089.6:c.826C>T	ENSP00000377649.2:p.Arg276Trp
ENST00000420042.1:n.502C>T
ENST00000425707.7:c.535C>T	ENSP00000389993.3:p.Arg179Trp
ENST00000475125.1:c.469C>T	ENSP00000462514.1:p.Arg157Trp
XM_005257552.3:c.874C>T	XP_005257609.1:p.Arg292Trp
XM_005257552.5:c.874C>T	XP_005257609.1:p.Arg292Trp
XM_005257553.1:c.826C>T	XP_005257610.1:p.Arg276Trp
XM_005257554.1:c.826C>T	XP_005257611.1:p.Arg276Trp
XM_011525095.1:c.826C>T	XP_011523397.1:p.Arg276Trp
XM_011525096.1:c.652C>T	XP_011523398.1:p.Arg218Trp
XM_017024920.2:c.469C>T	XP_016880409.1:p.Arg157Trp