Canonical Allele Identifier: CA2800892078

Gene: NRL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24081623_24081624insACA , CM000676.2:g.24081623_24081624insACA	GRCh38
NC_000014.8:g.24550832_24550833insACA , CM000676.1:g.24550832_24550833insACA	GRCh37
NC_000014.7:g.23620672_23620673insACA	NCBI36
NG_011697.1:g.8000_8001insTGT
NG_011697.2:g.38391_38392insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.382-56_382-55insTGT MANE Select	ENSP00000454062.2:n.382-56_382-55insTGT
ENST00000396995.1:c.-36-56_-36-55insTGT	ENSP00000380191.1:n.-36-56_-36-55insTGT
ENST00000396997.1:c.382-56_382-55insTGT	ENSP00000380193.1:n.382-56_382-55insTGT
ENST00000397002.6:c.382-56_382-55insTGT	ENSP00000380197.2:n.382-56_382-55insTGT
ENST00000560550.1:c.-36-56_-36-55insTGT	ENSP00000452966.1:n.-36-56_-36-55insTGT
ENST00000561028.5:c.382-56_382-55insTGT	ENSP00000454062.1:n.382-56_382-55insTGT
NM_006177.3:c.382-56_382-55insTGT	NP_006168.1:n.382-56_382-55insTGT
XM_005267708.3:c.382-56_382-55insTGT	XP_005267765.1:n.382-56_382-55insTGT
XM_005267709.3:c.382-56_382-55insTGT	XP_005267766.1:n.382-56_382-55insTGT
XM_005267710.3:c.382-56_382-55insTGT	XP_005267767.1:n.382-56_382-55insTGT
XM_011536801.1:c.481-56_481-55insTGT	XP_011535103.1:n.481-56_481-55insTGT
XM_011536802.1:c.382-56_382-55insTGT	XP_011535104.1:n.382-56_382-55insTGT
XM_011536803.1:c.382-56_382-55insTGT	XP_011535105.1:n.382-56_382-55insTGT
XM_011536804.1:c.382-56_382-55insTGT	XP_011535106.1:n.382-56_382-55insTGT
XM_011536805.1:c.382-56_382-55insTGT	XP_011535107.1:n.382-56_382-55insTGT
XM_011536806.1:c.166-56_166-55insTGT	XP_011535108.1:n.166-56_166-55insTGT
NM_001354768.1:c.382-56_382-55insTGT	NP_001341697.1:n.382-56_382-55insTGT
NM_001354769.1:c.382-56_382-55insTGT	NP_001341698.1:n.382-56_382-55insTGT
NM_001354770.1:c.67-56_67-55insTGT	NP_001341699.1:n.67-56_67-55insTGT
NM_006177.4:c.382-56_382-55insTGT	NP_006168.1:n.382-56_382-55insTGT
XM_011536801.2:c.688-56_688-55insTGT	XP_011535103.2:n.688-56_688-55insTGT
XM_011536804.2:c.382-56_382-55insTGT	XP_011535106.1:n.382-56_382-55insTGT
XM_011536805.2:c.382-56_382-55insTGT	XP_011535107.1:n.382-56_382-55insTGT
XM_011536806.2:c.373-56_373-55insTGT	XP_011535108.2:n.373-56_373-55insTGT
NM_001354768.3:c.382-56_382-55insTGT MANE Select	NP_001341697.1:n.382-56_382-55insTGT
NM_001354770.2:c.67-56_67-55insTGT	NP_001341699.1:n.67-56_67-55insTGT
NM_006177.5:c.382-56_382-55insTGT	NP_006168.1:n.382-56_382-55insTGT