Canonical Allele Identifier: CA2624298620

Gene: NRL

Linked Data

• gnomAD v4: 14-24081473-C-CGTG

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24081473_24081474insGTG , CM000676.2:g.24081473_24081474insGTG	GRCh38
NC_000014.8:g.24550682_24550683insGTG , CM000676.1:g.24550682_24550683insGTG	GRCh37
NC_000014.7:g.23620522_23620523insGTG	NCBI36
NG_011697.1:g.8150_8151insCAC
NG_011697.2:g.38541_38542insCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.476_477insCAC MANE Select	ENSP00000454062.2:p.Arg159_Leu160insThr
ENST00000396995.1:c.59_60insCAC	ENSP00000380191.1:p.Arg20_Leu21insThr
ENST00000396997.1:c.476_477insCAC	ENSP00000380193.1:p.Arg159_Leu160insThr
ENST00000397002.6:c.476_477insCAC	ENSP00000380197.2:p.Arg159_Leu160insThr
ENST00000560550.1:c.59_60insCAC	ENSP00000452966.1:p.Arg20_Leu21insThr
ENST00000561028.5:c.476_477insCAC	ENSP00000454062.1:p.Arg159_Leu160insThr
NM_006177.3:c.476_477insCAC	NP_006168.1:p.Arg159_Leu160insThr
XM_005267708.3:c.476_477insCAC	XP_005267765.1:p.Arg159_Leu160insThr
XM_005267709.3:c.476_477insCAC	XP_005267766.1:p.Arg159_Leu160insThr
XM_005267710.3:c.476_477insCAC	XP_005267767.1:p.Arg159_Leu160insThr
XM_011536801.1:c.575_576insCAC	XP_011535103.1:p.Arg192_Leu193insThr
XM_011536802.1:c.476_477insCAC	XP_011535104.1:p.Arg159_Leu160insThr
XM_011536803.1:c.476_477insCAC	XP_011535105.1:p.Arg159_Leu160insThr
XM_011536804.1:c.476_477insCAC	XP_011535106.1:p.Arg159_Leu160insThr
XM_011536805.1:c.476_477insCAC	XP_011535107.1:p.Arg159_Leu160insThr
XM_011536806.1:c.260_261insCAC	XP_011535108.1:p.Arg87_Leu88insThr
NM_001354768.1:c.476_477insCAC	NP_001341697.1:p.Arg159_Leu160insThr
NM_001354769.1:c.476_477insCAC	NP_001341698.1:p.Arg159_Leu160insThr
NM_001354770.1:c.161_162insCAC	NP_001341699.1:p.Arg54_Leu55insThr
NM_006177.4:c.476_477insCAC	NP_006168.1:p.Arg159_Leu160insThr
XM_011536801.2:c.782_783insCAC	XP_011535103.2:p.Arg261_Leu262insThr
XM_011536804.2:c.476_477insCAC	XP_011535106.1:p.Arg159_Leu160insThr
XM_011536805.2:c.476_477insCAC	XP_011535107.1:p.Arg159_Leu160insThr
XM_011536806.2:c.467_468insCAC	XP_011535108.2:p.Arg156_Leu157insThr
NM_001354768.3:c.476_477insCAC MANE Select	NP_001341697.1:p.Arg159_Leu160insThr
NM_001354770.2:c.161_162insCAC	NP_001341699.1:p.Arg54_Leu55insThr
NM_006177.5:c.476_477insCAC	NP_006168.1:p.Arg159_Leu160insThr