Canonical Allele Identifier: CA2800892048

Gene: NRL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24081200_24081201insTTCAGAATGAAAATA , CM000676.2:g.24081200_24081201insTTCAGAATGAAAATA	GRCh38
NC_000014.8:g.24550409_24550410insTTCAGAATGAAAATA , CM000676.1:g.24550409_24550410insTTCAGAATGAAAATA	GRCh37
NC_000014.7:g.23620249_23620250insTTCAGAATGAAAATA	NCBI36
NG_011697.1:g.8423_8424insTATTTTCATTCTGAA
NG_011697.2:g.38814_38815insTATTTTCATTCTGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.*35_*36insTATTTTCATTCTGAA MANE Select	ENSP00000454062.2:n.*35_*36insTATTTTCATTCTGAA
ENST00000396995.1:c.*35_*36insTATTTTCATTCTGAA	ENSP00000380191.1:n.*35_*36insTATTTTCATTCTGAA
ENST00000396997.1:c.*35_*36insTATTTTCATTCTGAA	ENSP00000380193.1:n.*35_*36insTATTTTCATTCTGAA
ENST00000397002.6:c.*35_*36insTATTTTCATTCTGAA	ENSP00000380197.2:n.*35_*36insTATTTTCATTCTGAA
ENST00000560550.1:c.*35_*36insTATTTTCATTCTGAA	ENSP00000452966.1:n.*35_*36insTATTTTCATTCTGAA
ENST00000561028.5:c.*35_*36insTATTTTCATTCTGAA	ENSP00000454062.1:n.*35_*36insTATTTTCATTCTGAA
NM_006177.3:c.*35_*36insTATTTTCATTCTGAA	NP_006168.1:n.*35_*36insTATTTTCATTCTGAA
XM_005267708.3:c.*35_*36insTATTTTCATTCTGAA	XP_005267765.1:n.*35_*36insTATTTTCATTCTGAA
XM_005267709.3:c.*35_*36insTATTTTCATTCTGAA	XP_005267766.1:n.*35_*36insTATTTTCATTCTGAA
XM_005267710.3:c.*35_*36insTATTTTCATTCTGAA	XP_005267767.1:n.*35_*36insTATTTTCATTCTGAA
XM_011536801.1:c.*35_*36insTATTTTCATTCTGAA	XP_011535103.1:n.*35_*36insTATTTTCATTCTGAA
XM_011536802.1:c.*35_*36insTATTTTCATTCTGAA	XP_011535104.1:n.*35_*36insTATTTTCATTCTGAA
XM_011536803.1:c.*35_*36insTATTTTCATTCTGAA	XP_011535105.1:n.*35_*36insTATTTTCATTCTGAA
XM_011536804.1:c.*35_*36insTATTTTCATTCTGAA	XP_011535106.1:n.*35_*36insTATTTTCATTCTGAA
XM_011536805.1:c.*35_*36insTATTTTCATTCTGAA	XP_011535107.1:n.*35_*36insTATTTTCATTCTGAA
XM_011536806.1:c.*35_*36insTATTTTCATTCTGAA	XP_011535108.1:n.*35_*36insTATTTTCATTCTGAA
NM_001354768.1:c.*35_*36insTATTTTCATTCTGAA	NP_001341697.1:n.*35_*36insTATTTTCATTCTGAA
NM_001354769.1:c.*35_*36insTATTTTCATTCTGAA	NP_001341698.1:n.*35_*36insTATTTTCATTCTGAA
NM_001354770.1:c.*35_*36insTATTTTCATTCTGAA	NP_001341699.1:n.*35_*36insTATTTTCATTCTGAA
NM_006177.4:c.*35_*36insTATTTTCATTCTGAA	NP_006168.1:n.*35_*36insTATTTTCATTCTGAA
XM_011536801.2:c.*35_*36insTATTTTCATTCTGAA	XP_011535103.2:n.*35_*36insTATTTTCATTCTGAA
XM_011536804.2:c.*35_*36insTATTTTCATTCTGAA	XP_011535106.1:n.*35_*36insTATTTTCATTCTGAA
XM_011536805.2:c.*35_*36insTATTTTCATTCTGAA	XP_011535107.1:n.*35_*36insTATTTTCATTCTGAA
XM_011536806.2:c.*35_*36insTATTTTCATTCTGAA	XP_011535108.2:n.*35_*36insTATTTTCATTCTGAA
NM_001354768.3:c.*35_*36insTATTTTCATTCTGAA MANE Select	NP_001341697.1:n.*35_*36insTATTTTCATTCTGAA
NM_001354770.2:c.*35_*36insTATTTTCATTCTGAA	NP_001341699.1:n.*35_*36insTATTTTCATTCTGAA
NM_006177.5:c.*35_*36insTATTTTCATTCTGAA	NP_006168.1:n.*35_*36insTATTTTCATTCTGAA