Canonical Allele Identifier: CA2123779319
Gene: NRL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24082417_24082424delinsGTCCTCCT , CM000676.2:g.24082417_24082424delinsGTCCTCCT GRCh38
NC_000014.8:g.24551626_24551633delinsGTCCTCCT , CM000676.1:g.24551626_24551633delinsGTCCTCCT GRCh37
NC_000014.7:g.23621466_23621473delinsGTCCTCCT NCBI36
NG_011697.1:g.7200_7207delinsAGGAGGAC
NG_011697.2:g.37591_37598delinsAGGAGGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000561028.6:c.381+44_381+51delinsAGGAGGAC MANE Select ENSP00000454062.2:n.381+44_381+51delinsAGGAGGAC
ENST00000396997.1:c.381+44_381+51delinsAGGAGGAC ENSP00000380193.1:n.381+44_381+51delinsAGGAGGAC
ENST00000397002.6:c.381+44_381+51delinsAGGAGGAC ENSP00000380197.2:n.381+44_381+51delinsAGGAGGAC
ENST00000561028.5:c.381+44_381+51delinsAGGAGGAC ENSP00000454062.1:n.381+44_381+51delinsAGGAGGAC
NM_006177.3:c.381+44_381+51delinsAGGAGGAC NP_006168.1:n.381+44_381+51delinsAGGAGGAC
XM_005267708.3:c.381+44_381+51delinsAGGAGGAC XP_005267765.1:n.381+44_381+51delinsAGGAGGAC
XM_005267709.3:c.381+44_381+51delinsAGGAGGAC XP_005267766.1:n.381+44_381+51delinsAGGAGGAC
XM_005267710.3:c.381+44_381+51delinsAGGAGGAC XP_005267767.1:n.381+44_381+51delinsAGGAGGAC
XM_011536801.1:c.480+44_480+51delinsAGGAGGAC XP_011535103.1:n.480+44_480+51delinsAGGAGGAC
XM_011536802.1:c.381+44_381+51delinsAGGAGGAC XP_011535104.1:n.381+44_381+51delinsAGGAGGAC
XM_011536803.1:c.381+44_381+51delinsAGGAGGAC XP_011535105.1:n.381+44_381+51delinsAGGAGGAC
XM_011536804.1:c.381+44_381+51delinsAGGAGGAC XP_011535106.1:n.381+44_381+51delinsAGGAGGAC
XM_011536805.1:c.381+44_381+51delinsAGGAGGAC XP_011535107.1:n.381+44_381+51delinsAGGAGGAC
XM_011536806.1:c.165+359_165+366delinsAGGAGGAC XP_011535108.1:n.165+359_165+366delinsAGGAGGAC
NM_001354768.1:c.381+44_381+51delinsAGGAGGAC NP_001341697.1:n.381+44_381+51delinsAGGAGGAC
NM_001354769.1:c.381+44_381+51delinsAGGAGGAC NP_001341698.1:n.381+44_381+51delinsAGGAGGAC
NM_001354770.1:c.66+359_66+366delinsAGGAGGAC NP_001341699.1:n.66+359_66+366delinsAGGAGGAC
NM_006177.4:c.381+44_381+51delinsAGGAGGAC NP_006168.1:n.381+44_381+51delinsAGGAGGAC
XM_011536801.2:c.687+44_687+51delinsAGGAGGAC XP_011535103.2:n.687+44_687+51delinsAGGAGGAC
XM_011536804.2:c.381+44_381+51delinsAGGAGGAC XP_011535106.1:n.381+44_381+51delinsAGGAGGAC
XM_011536805.2:c.381+44_381+51delinsAGGAGGAC XP_011535107.1:n.381+44_381+51delinsAGGAGGAC
XM_011536806.2:c.372+359_372+366delinsAGGAGGAC XP_011535108.2:n.372+359_372+366delinsAGGAGGAC
NM_001354768.3:c.381+44_381+51delinsAGGAGGAC MANE Select NP_001341697.1:n.381+44_381+51delinsAGGAGGAC
NM_001354770.2:c.66+359_66+366delinsAGGAGGAC NP_001341699.1:n.66+359_66+366delinsAGGAGGAC
NM_006177.5:c.381+44_381+51delinsAGGAGGAC NP_006168.1:n.381+44_381+51delinsAGGAGGAC