Canonical Allele Identifier: CA2800892077

Gene: NRL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24081619_24081620insAGT , CM000676.2:g.24081619_24081620insAGT	GRCh38
NC_000014.8:g.24550828_24550829insAGT , CM000676.1:g.24550828_24550829insAGT	GRCh37
NC_000014.7:g.23620668_23620669insAGT	NCBI36
NG_011697.1:g.8004_8005insACT
NG_011697.2:g.38395_38396insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.382-52_382-51insACT MANE Select	ENSP00000454062.2:n.382-52_382-51insACT
ENST00000396995.1:c.-36-52_-36-51insACT	ENSP00000380191.1:n.-36-52_-36-51insACT
ENST00000396997.1:c.382-52_382-51insACT	ENSP00000380193.1:n.382-52_382-51insACT
ENST00000397002.6:c.382-52_382-51insACT	ENSP00000380197.2:n.382-52_382-51insACT
ENST00000560550.1:c.-36-52_-36-51insACT	ENSP00000452966.1:n.-36-52_-36-51insACT
ENST00000561028.5:c.382-52_382-51insACT	ENSP00000454062.1:n.382-52_382-51insACT
NM_006177.3:c.382-52_382-51insACT	NP_006168.1:n.382-52_382-51insACT
XM_005267708.3:c.382-52_382-51insACT	XP_005267765.1:n.382-52_382-51insACT
XM_005267709.3:c.382-52_382-51insACT	XP_005267766.1:n.382-52_382-51insACT
XM_005267710.3:c.382-52_382-51insACT	XP_005267767.1:n.382-52_382-51insACT
XM_011536801.1:c.481-52_481-51insACT	XP_011535103.1:n.481-52_481-51insACT
XM_011536802.1:c.382-52_382-51insACT	XP_011535104.1:n.382-52_382-51insACT
XM_011536803.1:c.382-52_382-51insACT	XP_011535105.1:n.382-52_382-51insACT
XM_011536804.1:c.382-52_382-51insACT	XP_011535106.1:n.382-52_382-51insACT
XM_011536805.1:c.382-52_382-51insACT	XP_011535107.1:n.382-52_382-51insACT
XM_011536806.1:c.166-52_166-51insACT	XP_011535108.1:n.166-52_166-51insACT
NM_001354768.1:c.382-52_382-51insACT	NP_001341697.1:n.382-52_382-51insACT
NM_001354769.1:c.382-52_382-51insACT	NP_001341698.1:n.382-52_382-51insACT
NM_001354770.1:c.67-52_67-51insACT	NP_001341699.1:n.67-52_67-51insACT
NM_006177.4:c.382-52_382-51insACT	NP_006168.1:n.382-52_382-51insACT
XM_011536801.2:c.688-52_688-51insACT	XP_011535103.2:n.688-52_688-51insACT
XM_011536804.2:c.382-52_382-51insACT	XP_011535106.1:n.382-52_382-51insACT
XM_011536805.2:c.382-52_382-51insACT	XP_011535107.1:n.382-52_382-51insACT
XM_011536806.2:c.373-52_373-51insACT	XP_011535108.2:n.373-52_373-51insACT
NM_001354768.3:c.382-52_382-51insACT MANE Select	NP_001341697.1:n.382-52_382-51insACT
NM_001354770.2:c.67-52_67-51insACT	NP_001341699.1:n.67-52_67-51insACT
NM_006177.5:c.382-52_382-51insACT	NP_006168.1:n.382-52_382-51insACT