Canonical Allele Identifier: CA2123777258

Gene: NRL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24081280A= , CM000676.2:g.24081280A=	GRCh38
NC_000014.8:g.24550489A= , CM000676.1:g.24550489A=	GRCh37
NC_000014.7:g.23620329A=	NCBI36
NG_011697.1:g.8344T=
NG_011697.2:g.38735T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.670T= MANE Select	ENSP00000454062.2:p.Ser224=
ENST00000396995.1:c.253T=	ENSP00000380191.1:p.Ser85=
ENST00000396997.1:c.670T=	ENSP00000380193.1:p.Ser224=
ENST00000397002.6:c.670T=	ENSP00000380197.2:p.Ser224=
ENST00000560550.1:c.253T=	ENSP00000452966.1:p.Ser85=
ENST00000561028.5:c.670T=	ENSP00000454062.1:p.Ser224=
NM_006177.3:c.670T=	NP_006168.1:p.Ser224=
XM_005267708.3:c.670T=	XP_005267765.1:p.Ser224=
XM_005267709.3:c.670T=	XP_005267766.1:p.Ser224=
XM_005267710.3:c.670T=	XP_005267767.1:p.Ser224=
XM_011536801.1:c.769T=	XP_011535103.1:p.Ser257=
XM_011536802.1:c.670T=	XP_011535104.1:p.Ser224=
XM_011536803.1:c.670T=	XP_011535105.1:p.Ser224=
XM_011536804.1:c.670T=	XP_011535106.1:p.Ser224=
XM_011536805.1:c.670T=	XP_011535107.1:p.Ser224=
XM_011536806.1:c.454T=	XP_011535108.1:p.Ser152=
NM_001354768.1:c.670T=	NP_001341697.1:p.Ser224=
NM_001354769.1:c.670T=	NP_001341698.1:p.Ser224=
NM_001354770.1:c.355T=	NP_001341699.1:p.Ser119=
NM_006177.4:c.670T=	NP_006168.1:p.Ser224=
XM_011536801.2:c.976T=	XP_011535103.2:p.Ser326=
XM_011536804.2:c.670T=	XP_011535106.1:p.Ser224=
XM_011536805.2:c.670T=	XP_011535107.1:p.Ser224=
XM_011536806.2:c.661T=	XP_011535108.2:p.Ser221=
NM_001354768.3:c.670T= MANE Select	NP_001341697.1:p.Ser224=
NM_001354770.2:c.355T=	NP_001341699.1:p.Ser119=
NM_006177.5:c.670T=	NP_006168.1:p.Ser224=