Canonical Allele Identifier: CA2123779300

Gene: NRL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24082392G= , CM000676.2:g.24082392G=	GRCh38
NC_000014.8:g.24551601G= , CM000676.1:g.24551601G=	GRCh37
NC_000014.7:g.23621441G=	NCBI36
NG_011697.1:g.7232C=
NG_011697.2:g.37623C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.381+76C= MANE Select	ENSP00000454062.2:n.381+76C=
ENST00000396997.1:c.381+76C=	ENSP00000380193.1:n.381+76C=
ENST00000397002.6:c.381+76C=	ENSP00000380197.2:n.381+76C=
ENST00000561028.5:c.381+76C=	ENSP00000454062.1:n.381+76C=
NM_006177.3:c.381+76C=	NP_006168.1:n.381+76C=
XM_005267708.3:c.381+76C=	XP_005267765.1:n.381+76C=
XM_005267709.3:c.381+76C=	XP_005267766.1:n.381+76C=
XM_005267710.3:c.381+76C=	XP_005267767.1:n.381+76C=
XM_011536801.1:c.480+76C=	XP_011535103.1:n.480+76C=
XM_011536802.1:c.381+76C=	XP_011535104.1:n.381+76C=
XM_011536803.1:c.381+76C=	XP_011535105.1:n.381+76C=
XM_011536804.1:c.381+76C=	XP_011535106.1:n.381+76C=
XM_011536805.1:c.381+76C=	XP_011535107.1:n.381+76C=
XM_011536806.1:c.165+391C=	XP_011535108.1:n.165+391C=
NM_001354768.1:c.381+76C=	NP_001341697.1:n.381+76C=
NM_001354769.1:c.381+76C=	NP_001341698.1:n.381+76C=
NM_001354770.1:c.66+391C=	NP_001341699.1:n.66+391C=
NM_006177.4:c.381+76C=	NP_006168.1:n.381+76C=
XM_011536801.2:c.687+76C=	XP_011535103.2:n.687+76C=
XM_011536804.2:c.381+76C=	XP_011535106.1:n.381+76C=
XM_011536805.2:c.381+76C=	XP_011535107.1:n.381+76C=
XM_011536806.2:c.372+391C=	XP_011535108.2:n.372+391C=
NM_001354768.3:c.381+76C= MANE Select	NP_001341697.1:n.381+76C=
NM_001354770.2:c.66+391C=	NP_001341699.1:n.66+391C=
NM_006177.5:c.381+76C=	NP_006168.1:n.381+76C=