Canonical Allele Identifier: CA2123777511

Gene: NRL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24081382C= , CM000676.2:g.24081382C=	GRCh38
NC_000014.8:g.24550591C= , CM000676.1:g.24550591C=	GRCh37
NC_000014.7:g.23620431C=	NCBI36
NG_011697.1:g.8242G=
NG_011697.2:g.38633G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.568G= MANE Select	ENSP00000454062.2:p.Glu190=
ENST00000396995.1:c.151G=	ENSP00000380191.1:p.Glu51=
ENST00000396997.1:c.568G=	ENSP00000380193.1:p.Glu190=
ENST00000397002.6:c.568G=	ENSP00000380197.2:p.Glu190=
ENST00000560550.1:c.151G=	ENSP00000452966.1:p.Glu51=
ENST00000561028.5:c.568G=	ENSP00000454062.1:p.Glu190=
NM_006177.3:c.568G=	NP_006168.1:p.Glu190=
XM_005267708.3:c.568G=	XP_005267765.1:p.Glu190=
XM_005267709.3:c.568G=	XP_005267766.1:p.Glu190=
XM_005267710.3:c.568G=	XP_005267767.1:p.Glu190=
XM_011536801.1:c.667G=	XP_011535103.1:p.Glu223=
XM_011536802.1:c.568G=	XP_011535104.1:p.Glu190=
XM_011536803.1:c.568G=	XP_011535105.1:p.Glu190=
XM_011536804.1:c.568G=	XP_011535106.1:p.Glu190=
XM_011536805.1:c.568G=	XP_011535107.1:p.Glu190=
XM_011536806.1:c.352G=	XP_011535108.1:p.Glu118=
NM_001354768.1:c.568G=	NP_001341697.1:p.Glu190=
NM_001354769.1:c.568G=	NP_001341698.1:p.Glu190=
NM_001354770.1:c.253G=	NP_001341699.1:p.Glu85=
NM_006177.4:c.568G=	NP_006168.1:p.Glu190=
XM_011536801.2:c.874G=	XP_011535103.2:p.Glu292=
XM_011536804.2:c.568G=	XP_011535106.1:p.Glu190=
XM_011536805.2:c.568G=	XP_011535107.1:p.Glu190=
XM_011536806.2:c.559G=	XP_011535108.2:p.Glu187=
NM_001354768.3:c.568G= MANE Select	NP_001341697.1:p.Glu190=
NM_001354770.2:c.253G=	NP_001341699.1:p.Glu85=
NM_006177.5:c.568G=	NP_006168.1:p.Glu190=