Canonical Allele Identifier: CA2123777269

Gene: NRL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24081282G= , CM000676.2:g.24081282G=	GRCh38
NC_000014.8:g.24550491G= , CM000676.1:g.24550491G=	GRCh37
NC_000014.7:g.23620331G=	NCBI36
NG_011697.1:g.8342C=
NG_011697.2:g.38733C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.668C= MANE Select	ENSP00000454062.2:p.Thr223=
ENST00000396995.1:c.251C=	ENSP00000380191.1:p.Thr84=
ENST00000396997.1:c.668C=	ENSP00000380193.1:p.Thr223=
ENST00000397002.6:c.668C=	ENSP00000380197.2:p.Thr223=
ENST00000560550.1:c.251C=	ENSP00000452966.1:p.Thr84=
ENST00000561028.5:c.668C=	ENSP00000454062.1:p.Thr223=
NM_006177.3:c.668C=	NP_006168.1:p.Thr223=
XM_005267708.3:c.668C=	XP_005267765.1:p.Thr223=
XM_005267709.3:c.668C=	XP_005267766.1:p.Thr223=
XM_005267710.3:c.668C=	XP_005267767.1:p.Thr223=
XM_011536801.1:c.767C=	XP_011535103.1:p.Thr256=
XM_011536802.1:c.668C=	XP_011535104.1:p.Thr223=
XM_011536803.1:c.668C=	XP_011535105.1:p.Thr223=
XM_011536804.1:c.668C=	XP_011535106.1:p.Thr223=
XM_011536805.1:c.668C=	XP_011535107.1:p.Thr223=
XM_011536806.1:c.452C=	XP_011535108.1:p.Thr151=
NM_001354768.1:c.668C=	NP_001341697.1:p.Thr223=
NM_001354769.1:c.668C=	NP_001341698.1:p.Thr223=
NM_001354770.1:c.353C=	NP_001341699.1:p.Thr118=
NM_006177.4:c.668C=	NP_006168.1:p.Thr223=
XM_011536801.2:c.974C=	XP_011535103.2:p.Thr325=
XM_011536804.2:c.668C=	XP_011535106.1:p.Thr223=
XM_011536805.2:c.668C=	XP_011535107.1:p.Thr223=
XM_011536806.2:c.659C=	XP_011535108.2:p.Thr220=
NM_001354768.3:c.668C= MANE Select	NP_001341697.1:p.Thr223=
NM_001354770.2:c.353C=	NP_001341699.1:p.Thr118=
NM_006177.5:c.668C=	NP_006168.1:p.Thr223=