Canonical Allele Identifier: CA2123777577

Gene: NRL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24081405_24081433delinsTGCAGCCGCTTGGAGCGACAGGCCTGCGC , CM000676.2:g.24081405_24081433delinsTGCAGCCGCTTGGAGCGACAGGCCTGCGC	GRCh38
NC_000014.8:g.24550614_24550642delinsTGCAGCCGCTTGGAGCGACAGGCCTGCGC , CM000676.1:g.24550614_24550642delinsTGCAGCCGCTTGGAGCGACAGGCCTGCGC	GRCh37
NC_000014.7:g.23620454_23620482delinsTGCAGCCGCTTGGAGCGACAGGCCTGCGC	NCBI36
NG_011697.1:g.8191_8219delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA
NG_011697.2:g.38582_38610delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.517_545delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA MANE Select	ENSP00000454062.2:p.Ala173=
ENST00000396995.1:c.100_128delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	ENSP00000380191.1:p.Ala34=
ENST00000396997.1:c.517_545delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	ENSP00000380193.1:p.Ala173=
ENST00000397002.6:c.517_545delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	ENSP00000380197.2:p.Ala173=
ENST00000560550.1:c.100_128delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	ENSP00000452966.1:p.Ala34=
ENST00000561028.5:c.517_545delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	ENSP00000454062.1:p.Ala173=
NM_006177.3:c.517_545delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	NP_006168.1:p.Ala173=
XM_005267708.3:c.517_545delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	XP_005267765.1:p.Ala173=
XM_005267709.3:c.517_545delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	XP_005267766.1:p.Ala173=
XM_005267710.3:c.517_545delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	XP_005267767.1:p.Ala173=
XM_011536801.1:c.616_644delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	XP_011535103.1:p.Ala206=
XM_011536802.1:c.517_545delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	XP_011535104.1:p.Ala173=
XM_011536803.1:c.517_545delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	XP_011535105.1:p.Ala173=
XM_011536804.1:c.517_545delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	XP_011535106.1:p.Ala173=
XM_011536805.1:c.517_545delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	XP_011535107.1:p.Ala173=
XM_011536806.1:c.301_329delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	XP_011535108.1:p.Ala101=
NM_001354768.1:c.517_545delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	NP_001341697.1:p.Ala173=
NM_001354769.1:c.517_545delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	NP_001341698.1:p.Ala173=
NM_001354770.1:c.202_230delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	NP_001341699.1:p.Ala68=
NM_006177.4:c.517_545delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	NP_006168.1:p.Ala173=
XM_011536801.2:c.823_851delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	XP_011535103.2:p.Ala275=
XM_011536804.2:c.517_545delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	XP_011535106.1:p.Ala173=
XM_011536805.2:c.517_545delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	XP_011535107.1:p.Ala173=
XM_011536806.2:c.508_536delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	XP_011535108.2:p.Ala170=
NM_001354768.3:c.517_545delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA MANE Select	NP_001341697.1:p.Ala173=
NM_001354770.2:c.202_230delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	NP_001341699.1:p.Ala68=
NM_006177.5:c.517_545delinsGCGCAGGCCTGTCGCTCCAAGCGGCTGCA	NP_006168.1:p.Ala173=