Canonical Allele Identifier: CA2123777599

Gene: NRL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24081410C= , CM000676.2:g.24081410C=	GRCh38
NC_000014.8:g.24550619C= , CM000676.1:g.24550619C=	GRCh37
NC_000014.7:g.23620459C=	NCBI36
NG_011697.1:g.8214G=
NG_011697.2:g.38605G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.540G= MANE Select	ENSP00000454062.2:p.Arg180=
ENST00000396995.1:c.123G=	ENSP00000380191.1:p.Arg41=
ENST00000396997.1:c.540G=	ENSP00000380193.1:p.Arg180=
ENST00000397002.6:c.540G=	ENSP00000380197.2:p.Arg180=
ENST00000560550.1:c.123G=	ENSP00000452966.1:p.Arg41=
ENST00000561028.5:c.540G=	ENSP00000454062.1:p.Arg180=
NM_006177.3:c.540G=	NP_006168.1:p.Arg180=
XM_005267708.3:c.540G=	XP_005267765.1:p.Arg180=
XM_005267709.3:c.540G=	XP_005267766.1:p.Arg180=
XM_005267710.3:c.540G=	XP_005267767.1:p.Arg180=
XM_011536801.1:c.639G=	XP_011535103.1:p.Arg213=
XM_011536802.1:c.540G=	XP_011535104.1:p.Arg180=
XM_011536803.1:c.540G=	XP_011535105.1:p.Arg180=
XM_011536804.1:c.540G=	XP_011535106.1:p.Arg180=
XM_011536805.1:c.540G=	XP_011535107.1:p.Arg180=
XM_011536806.1:c.324G=	XP_011535108.1:p.Arg108=
NM_001354768.1:c.540G=	NP_001341697.1:p.Arg180=
NM_001354769.1:c.540G=	NP_001341698.1:p.Arg180=
NM_001354770.1:c.225G=	NP_001341699.1:p.Arg75=
NM_006177.4:c.540G=	NP_006168.1:p.Arg180=
XM_011536801.2:c.846G=	XP_011535103.2:p.Arg282=
XM_011536804.2:c.540G=	XP_011535106.1:p.Arg180=
XM_011536805.2:c.540G=	XP_011535107.1:p.Arg180=
XM_011536806.2:c.531G=	XP_011535108.2:p.Arg177=
NM_001354768.3:c.540G= MANE Select	NP_001341697.1:p.Arg180=
NM_001354770.2:c.225G=	NP_001341699.1:p.Arg75=
NM_006177.5:c.540G=	NP_006168.1:p.Arg180=