Canonical Allele Identifier: CA2123777802

Gene: NRL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24081482C= , CM000676.2:g.24081482C=	GRCh38
NC_000014.8:g.24550691C= , CM000676.1:g.24550691C=	GRCh37
NC_000014.7:g.23620531C=	NCBI36
NG_011697.1:g.8142G=
NG_011697.2:g.38533G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.468G= MANE Select	ENSP00000454062.2:p.Glu156=
ENST00000396995.1:c.51G=	ENSP00000380191.1:p.Glu17=
ENST00000396997.1:c.468G=	ENSP00000380193.1:p.Glu156=
ENST00000397002.6:c.468G=	ENSP00000380197.2:p.Glu156=
ENST00000560550.1:c.51G=	ENSP00000452966.1:p.Glu17=
ENST00000561028.5:c.468G=	ENSP00000454062.1:p.Glu156=
NM_006177.3:c.468G=	NP_006168.1:p.Glu156=
XM_005267708.3:c.468G=	XP_005267765.1:p.Glu156=
XM_005267709.3:c.468G=	XP_005267766.1:p.Glu156=
XM_005267710.3:c.468G=	XP_005267767.1:p.Glu156=
XM_011536801.1:c.567G=	XP_011535103.1:p.Glu189=
XM_011536802.1:c.468G=	XP_011535104.1:p.Glu156=
XM_011536803.1:c.468G=	XP_011535105.1:p.Glu156=
XM_011536804.1:c.468G=	XP_011535106.1:p.Glu156=
XM_011536805.1:c.468G=	XP_011535107.1:p.Glu156=
XM_011536806.1:c.252G=	XP_011535108.1:p.Glu84=
NM_001354768.1:c.468G=	NP_001341697.1:p.Glu156=
NM_001354769.1:c.468G=	NP_001341698.1:p.Glu156=
NM_001354770.1:c.153G=	NP_001341699.1:p.Glu51=
NM_006177.4:c.468G=	NP_006168.1:p.Glu156=
XM_011536801.2:c.774G=	XP_011535103.2:p.Glu258=
XM_011536804.2:c.468G=	XP_011535106.1:p.Glu156=
XM_011536805.2:c.468G=	XP_011535107.1:p.Glu156=
XM_011536806.2:c.459G=	XP_011535108.2:p.Glu153=
NM_001354768.3:c.468G= MANE Select	NP_001341697.1:p.Glu156=
NM_001354770.2:c.153G=	NP_001341699.1:p.Glu51=
NM_006177.5:c.468G=	NP_006168.1:p.Glu156=