Canonical Allele Identifier: CA2123777498

Gene: NRL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24081375G= , CM000676.2:g.24081375G=	GRCh38
NC_000014.8:g.24550584G= , CM000676.1:g.24550584G=	GRCh37
NC_000014.7:g.23620424G=	NCBI36
NG_011697.1:g.8249C=
NG_011697.2:g.38640C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.575C= MANE Select	ENSP00000454062.2:p.Ala192=
ENST00000396995.1:c.158C=	ENSP00000380191.1:p.Ala53=
ENST00000396997.1:c.575C=	ENSP00000380193.1:p.Ala192=
ENST00000397002.6:c.575C=	ENSP00000380197.2:p.Ala192=
ENST00000560550.1:c.158C=	ENSP00000452966.1:p.Ala53=
ENST00000561028.5:c.575C=	ENSP00000454062.1:p.Ala192=
NM_006177.3:c.575C=	NP_006168.1:p.Ala192=
XM_005267708.3:c.575C=	XP_005267765.1:p.Ala192=
XM_005267709.3:c.575C=	XP_005267766.1:p.Ala192=
XM_005267710.3:c.575C=	XP_005267767.1:p.Ala192=
XM_011536801.1:c.674C=	XP_011535103.1:p.Ala225=
XM_011536802.1:c.575C=	XP_011535104.1:p.Ala192=
XM_011536803.1:c.575C=	XP_011535105.1:p.Ala192=
XM_011536804.1:c.575C=	XP_011535106.1:p.Ala192=
XM_011536805.1:c.575C=	XP_011535107.1:p.Ala192=
XM_011536806.1:c.359C=	XP_011535108.1:p.Ala120=
NM_001354768.1:c.575C=	NP_001341697.1:p.Ala192=
NM_001354769.1:c.575C=	NP_001341698.1:p.Ala192=
NM_001354770.1:c.260C=	NP_001341699.1:p.Ala87=
NM_006177.4:c.575C=	NP_006168.1:p.Ala192=
XM_011536801.2:c.881C=	XP_011535103.2:p.Ala294=
XM_011536804.2:c.575C=	XP_011535106.1:p.Ala192=
XM_011536805.2:c.575C=	XP_011535107.1:p.Ala192=
XM_011536806.2:c.566C=	XP_011535108.2:p.Ala189=
NM_001354768.3:c.575C= MANE Select	NP_001341697.1:p.Ala192=
NM_001354770.2:c.260C=	NP_001341699.1:p.Ala87=
NM_006177.5:c.575C=	NP_006168.1:p.Ala192=