Canonical Allele Identifier: CA2123777720

Gene: NRL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24081457_24081477delinsGGCGCCTCTGCTTCAGCCGCA , CM000676.2:g.24081457_24081477delinsGGCGCCTCTGCTTCAGCCGCA	GRCh38
NC_000014.8:g.24550666_24550686delinsGGCGCCTCTGCTTCAGCCGCA , CM000676.1:g.24550666_24550686delinsGGCGCCTCTGCTTCAGCCGCA	GRCh37
NC_000014.7:g.23620506_23620526delinsGGCGCCTCTGCTTCAGCCGCA	NCBI36
NG_011697.1:g.8147_8167delinsTGCGGCTGAAGCAGAGGCGCC
NG_011697.2:g.38538_38558delinsTGCGGCTGAAGCAGAGGCGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.473_493delinsTGCGGCTGAAGCAGAGGCGCC MANE Select	ENSP00000454062.2:p.Leu158=
ENST00000396995.1:c.56_76delinsTGCGGCTGAAGCAGAGGCGCC	ENSP00000380191.1:p.Leu19=
ENST00000396997.1:c.473_493delinsTGCGGCTGAAGCAGAGGCGCC	ENSP00000380193.1:p.Leu158=
ENST00000397002.6:c.473_493delinsTGCGGCTGAAGCAGAGGCGCC	ENSP00000380197.2:p.Leu158=
ENST00000560550.1:c.56_76delinsTGCGGCTGAAGCAGAGGCGCC	ENSP00000452966.1:p.Leu19=
ENST00000561028.5:c.473_493delinsTGCGGCTGAAGCAGAGGCGCC	ENSP00000454062.1:p.Leu158=
NM_006177.3:c.473_493delinsTGCGGCTGAAGCAGAGGCGCC	NP_006168.1:p.Leu158=
XM_005267708.3:c.473_493delinsTGCGGCTGAAGCAGAGGCGCC	XP_005267765.1:p.Leu158=
XM_005267709.3:c.473_493delinsTGCGGCTGAAGCAGAGGCGCC	XP_005267766.1:p.Leu158=
XM_005267710.3:c.473_493delinsTGCGGCTGAAGCAGAGGCGCC	XP_005267767.1:p.Leu158=
XM_011536801.1:c.572_592delinsTGCGGCTGAAGCAGAGGCGCC	XP_011535103.1:p.Leu191=
XM_011536802.1:c.473_493delinsTGCGGCTGAAGCAGAGGCGCC	XP_011535104.1:p.Leu158=
XM_011536803.1:c.473_493delinsTGCGGCTGAAGCAGAGGCGCC	XP_011535105.1:p.Leu158=
XM_011536804.1:c.473_493delinsTGCGGCTGAAGCAGAGGCGCC	XP_011535106.1:p.Leu158=
XM_011536805.1:c.473_493delinsTGCGGCTGAAGCAGAGGCGCC	XP_011535107.1:p.Leu158=
XM_011536806.1:c.257_277delinsTGCGGCTGAAGCAGAGGCGCC	XP_011535108.1:p.Leu86=
NM_001354768.1:c.473_493delinsTGCGGCTGAAGCAGAGGCGCC	NP_001341697.1:p.Leu158=
NM_001354769.1:c.473_493delinsTGCGGCTGAAGCAGAGGCGCC	NP_001341698.1:p.Leu158=
NM_001354770.1:c.158_178delinsTGCGGCTGAAGCAGAGGCGCC	NP_001341699.1:p.Leu53=
NM_006177.4:c.473_493delinsTGCGGCTGAAGCAGAGGCGCC	NP_006168.1:p.Leu158=
XM_011536801.2:c.779_799delinsTGCGGCTGAAGCAGAGGCGCC	XP_011535103.2:p.Leu260=
XM_011536804.2:c.473_493delinsTGCGGCTGAAGCAGAGGCGCC	XP_011535106.1:p.Leu158=
XM_011536805.2:c.473_493delinsTGCGGCTGAAGCAGAGGCGCC	XP_011535107.1:p.Leu158=
XM_011536806.2:c.464_484delinsTGCGGCTGAAGCAGAGGCGCC	XP_011535108.2:p.Leu155=
NM_001354768.3:c.473_493delinsTGCGGCTGAAGCAGAGGCGCC MANE Select	NP_001341697.1:p.Leu158=
NM_001354770.2:c.158_178delinsTGCGGCTGAAGCAGAGGCGCC	NP_001341699.1:p.Leu53=
NM_006177.5:c.473_493delinsTGCGGCTGAAGCAGAGGCGCC	NP_006168.1:p.Leu158=