Canonical Allele Identifier: CA2624301101

Gene: NRL

Linked Data

• gnomAD v4: 14-24082480-GGCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24082481_24082483del , CM000676.2:g.24082481_24082483del	GRCh38
NC_000014.8:g.24551690_24551692del , CM000676.1:g.24551690_24551692del	GRCh37
NC_000014.7:g.23621530_23621532del	NCBI36
NG_011697.1:g.7141_7143del
NG_011697.2:g.37532_37534del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.366_368del MANE Select	ENSP00000454062.2:p.Ala123del
ENST00000396997.1:c.366_368del	ENSP00000380193.1:p.Ala123del
ENST00000397002.6:c.366_368del	ENSP00000380197.2:p.Ala123del
ENST00000561028.5:c.366_368del	ENSP00000454062.1:p.Ala123del
NM_006177.3:c.366_368del	NP_006168.1:p.Ala123del
XM_005267708.3:c.366_368del	XP_005267765.1:p.Ala123del
XM_005267709.3:c.366_368del	XP_005267766.1:p.Ala123del
XM_005267710.3:c.366_368del	XP_005267767.1:p.Ala123del
XM_011536801.1:c.465_467del	XP_011535103.1:p.Ala156del
XM_011536802.1:c.366_368del	XP_011535104.1:p.Ala123del
XM_011536803.1:c.366_368del	XP_011535105.1:p.Ala123del
XM_011536804.1:c.366_368del	XP_011535106.1:p.Ala123del
XM_011536805.1:c.366_368del	XP_011535107.1:p.Ala123del
XM_011536806.1:c.165+300_165+302del	XP_011535108.1:n.165+300_165+302del
NM_001354768.1:c.366_368del	NP_001341697.1:p.Ala123del
NM_001354769.1:c.366_368del	NP_001341698.1:p.Ala123del
NM_001354770.1:c.66+300_66+302del	NP_001341699.1:n.66+300_66+302del
NM_006177.4:c.366_368del	NP_006168.1:p.Ala123del
XM_011536801.2:c.672_674del	XP_011535103.2:p.Ala225del
XM_011536804.2:c.366_368del	XP_011535106.1:p.Ala123del
XM_011536805.2:c.366_368del	XP_011535107.1:p.Ala123del
XM_011536806.2:c.372+300_372+302del	XP_011535108.2:n.372+300_372+302del
NM_001354768.3:c.366_368del MANE Select	NP_001341697.1:p.Ala123del
NM_001354770.2:c.66+300_66+302del	NP_001341699.1:n.66+300_66+302del
NM_006177.5:c.366_368del	NP_006168.1:p.Ala123del