Canonical Allele Identifier: CA2123779500

Gene: NRL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24082578_24082595delinsTCAGCCCCAATGCCTCCC , CM000676.2:g.24082578_24082595delinsTCAGCCCCAATGCCTCCC	GRCh38
NC_000014.8:g.24551787_24551804delinsTCAGCCCCAATGCCTCCC , CM000676.1:g.24551787_24551804delinsTCAGCCCCAATGCCTCCC	GRCh37
NC_000014.7:g.23621627_23621644delinsTCAGCCCCAATGCCTCCC	NCBI36
NG_011697.1:g.7029_7046delinsGGGAGGCATTGGGGCTGA
NG_011697.2:g.37420_37437delinsGGGAGGCATTGGGGCTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.254_271delinsGGGAGGCATTGGGGCTGA MANE Select	ENSP00000454062.2:p.Gly85=
ENST00000396997.1:c.254_271delinsGGGAGGCATTGGGGCTGA	ENSP00000380193.1:p.Gly85=
ENST00000397002.6:c.254_271delinsGGGAGGCATTGGGGCTGA	ENSP00000380197.2:p.Gly85=
ENST00000561028.5:c.254_271delinsGGGAGGCATTGGGGCTGA	ENSP00000454062.1:p.Gly85=
NM_006177.3:c.254_271delinsGGGAGGCATTGGGGCTGA	NP_006168.1:p.Gly85=
XM_005267708.3:c.254_271delinsGGGAGGCATTGGGGCTGA	XP_005267765.1:p.Gly85=
XM_005267709.3:c.254_271delinsGGGAGGCATTGGGGCTGA	XP_005267766.1:p.Gly85=
XM_005267710.3:c.254_271delinsGGGAGGCATTGGGGCTGA	XP_005267767.1:p.Gly85=
XM_011536801.1:c.353_370delinsGGGAGGCATTGGGGCTGA	XP_011535103.1:p.Gly118=
XM_011536802.1:c.254_271delinsGGGAGGCATTGGGGCTGA	XP_011535104.1:p.Gly85=
XM_011536803.1:c.254_271delinsGGGAGGCATTGGGGCTGA	XP_011535105.1:p.Gly85=
XM_011536804.1:c.254_271delinsGGGAGGCATTGGGGCTGA	XP_011535106.1:p.Gly85=
XM_011536805.1:c.254_271delinsGGGAGGCATTGGGGCTGA	XP_011535107.1:p.Gly85=
XM_011536806.1:c.165+188_165+205delinsGGGAGGCATTGGGGCTGA	XP_011535108.1:n.165+188_165+205delinsGGGAGGCATTGGGGCTGA
NM_001354768.1:c.254_271delinsGGGAGGCATTGGGGCTGA	NP_001341697.1:p.Gly85=
NM_001354769.1:c.254_271delinsGGGAGGCATTGGGGCTGA	NP_001341698.1:p.Gly85=
NM_001354770.1:c.66+188_66+205delinsGGGAGGCATTGGGGCTGA	NP_001341699.1:n.66+188_66+205delinsGGGAGGCATTGGGGCTGA
NM_006177.4:c.254_271delinsGGGAGGCATTGGGGCTGA	NP_006168.1:p.Gly85=
XM_011536801.2:c.560_577delinsGGGAGGCATTGGGGCTGA	XP_011535103.2:p.Gly187=
XM_011536804.2:c.254_271delinsGGGAGGCATTGGGGCTGA	XP_011535106.1:p.Gly85=
XM_011536805.2:c.254_271delinsGGGAGGCATTGGGGCTGA	XP_011535107.1:p.Gly85=
XM_011536806.2:c.372+188_372+205delinsGGGAGGCATTGGGGCTGA	XP_011535108.2:n.372+188_372+205delinsGGGAGGCATTGGGGCTGA
NM_001354768.3:c.254_271delinsGGGAGGCATTGGGGCTGA MANE Select	NP_001341697.1:p.Gly85=
NM_001354770.2:c.66+188_66+205delinsGGGAGGCATTGGGGCTGA	NP_001341699.1:n.66+188_66+205delinsGGGAGGCATTGGGGCTGA
NM_006177.5:c.254_271delinsGGGAGGCATTGGGGCTGA	NP_006168.1:p.Gly85=