Canonical Allele Identifier: CA2800892057

Gene: NRL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24081558_24081559insACA , CM000676.2:g.24081558_24081559insACA	GRCh38
NC_000014.8:g.24550767_24550768insACA , CM000676.1:g.24550767_24550768insACA	GRCh37
NC_000014.7:g.23620607_23620608insACA	NCBI36
NG_011697.1:g.8065_8066insTGT
NG_011697.2:g.38456_38457insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.391_392insTGT MANE Select	ENSP00000454062.2:p.Arg131delinsLeuTrp
ENST00000396995.1:c.-27_-26insTGT	ENSP00000380191.1:n.-27_-26insTGT
ENST00000396997.1:c.391_392insTGT	ENSP00000380193.1:p.Arg131delinsLeuTrp
ENST00000397002.6:c.391_392insTGT	ENSP00000380197.2:p.Arg131delinsLeuTrp
ENST00000560550.1:c.-27_-26insTGT	ENSP00000452966.1:n.-27_-26insTGT
ENST00000561028.5:c.391_392insTGT	ENSP00000454062.1:p.Arg131delinsLeuTrp
NM_006177.3:c.391_392insTGT	NP_006168.1:p.Arg131delinsLeuTrp
XM_005267708.3:c.391_392insTGT	XP_005267765.1:p.Arg131delinsLeuTrp
XM_005267709.3:c.391_392insTGT	XP_005267766.1:p.Arg131delinsLeuTrp
XM_005267710.3:c.391_392insTGT	XP_005267767.1:p.Arg131delinsLeuTrp
XM_011536801.1:c.490_491insTGT	XP_011535103.1:p.Arg164delinsLeuTrp
XM_011536802.1:c.391_392insTGT	XP_011535104.1:p.Arg131delinsLeuTrp
XM_011536803.1:c.391_392insTGT	XP_011535105.1:p.Arg131delinsLeuTrp
XM_011536804.1:c.391_392insTGT	XP_011535106.1:p.Arg131delinsLeuTrp
XM_011536805.1:c.391_392insTGT	XP_011535107.1:p.Arg131delinsLeuTrp
XM_011536806.1:c.175_176insTGT	XP_011535108.1:p.Arg59delinsLeuTrp
NM_001354768.1:c.391_392insTGT	NP_001341697.1:p.Arg131delinsLeuTrp
NM_001354769.1:c.391_392insTGT	NP_001341698.1:p.Arg131delinsLeuTrp
NM_001354770.1:c.76_77insTGT	NP_001341699.1:p.Arg26delinsLeuTrp
NM_006177.4:c.391_392insTGT	NP_006168.1:p.Arg131delinsLeuTrp
XM_011536801.2:c.697_698insTGT	XP_011535103.2:p.Arg233delinsLeuTrp
XM_011536804.2:c.391_392insTGT	XP_011535106.1:p.Arg131delinsLeuTrp
XM_011536805.2:c.391_392insTGT	XP_011535107.1:p.Arg131delinsLeuTrp
XM_011536806.2:c.382_383insTGT	XP_011535108.2:p.Arg128delinsLeuTrp
NM_001354768.3:c.391_392insTGT MANE Select	NP_001341697.1:p.Arg131delinsLeuTrp
NM_001354770.2:c.76_77insTGT	NP_001341699.1:p.Arg26delinsLeuTrp
NM_006177.5:c.391_392insTGT	NP_006168.1:p.Arg131delinsLeuTrp