Canonical Allele Identifier: CA2123777724

Gene: NRL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24081461C= , CM000676.2:g.24081461C=	GRCh38
NC_000014.8:g.24550670C= , CM000676.1:g.24550670C=	GRCh37
NC_000014.7:g.23620510C=	NCBI36
NG_011697.1:g.8163G=
NG_011697.2:g.38554G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.489G= MANE Select	ENSP00000454062.2:p.Arg163=
ENST00000396995.1:c.72G=	ENSP00000380191.1:p.Arg24=
ENST00000396997.1:c.489G=	ENSP00000380193.1:p.Arg163=
ENST00000397002.6:c.489G=	ENSP00000380197.2:p.Arg163=
ENST00000560550.1:c.72G=	ENSP00000452966.1:p.Arg24=
ENST00000561028.5:c.489G=	ENSP00000454062.1:p.Arg163=
NM_006177.3:c.489G=	NP_006168.1:p.Arg163=
XM_005267708.3:c.489G=	XP_005267765.1:p.Arg163=
XM_005267709.3:c.489G=	XP_005267766.1:p.Arg163=
XM_005267710.3:c.489G=	XP_005267767.1:p.Arg163=
XM_011536801.1:c.588G=	XP_011535103.1:p.Arg196=
XM_011536802.1:c.489G=	XP_011535104.1:p.Arg163=
XM_011536803.1:c.489G=	XP_011535105.1:p.Arg163=
XM_011536804.1:c.489G=	XP_011535106.1:p.Arg163=
XM_011536805.1:c.489G=	XP_011535107.1:p.Arg163=
XM_011536806.1:c.273G=	XP_011535108.1:p.Arg91=
NM_001354768.1:c.489G=	NP_001341697.1:p.Arg163=
NM_001354769.1:c.489G=	NP_001341698.1:p.Arg163=
NM_001354770.1:c.174G=	NP_001341699.1:p.Arg58=
NM_006177.4:c.489G=	NP_006168.1:p.Arg163=
XM_011536801.2:c.795G=	XP_011535103.2:p.Arg265=
XM_011536804.2:c.489G=	XP_011535106.1:p.Arg163=
XM_011536805.2:c.489G=	XP_011535107.1:p.Arg163=
XM_011536806.2:c.480G=	XP_011535108.2:p.Arg160=
NM_001354768.3:c.489G= MANE Select	NP_001341697.1:p.Arg163=
NM_001354770.2:c.174G=	NP_001341699.1:p.Arg58=
NM_006177.5:c.489G=	NP_006168.1:p.Arg163=