Canonical Allele Identifier: CA10634761

Gene: NRL

Linked Data

• ClinVar Variation Id: 312934
• ClinVar RCV Id: RCV000271600
• dbSNP Id: rs200281199
• gnomAD v2: 14-24550161-AC-A
• gnomAD v3: 14-24080952-AC-A
• gnomAD v4: 14-24080952-AC-A
• MyVariant Identifiers: chr14:g.24550162del (hg19) ; chr14:g.24080953del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24080958del , CM000676.2:g.24080958del	GRCh38
NC_000014.8:g.24550167del , CM000676.1:g.24550167del	GRCh37
NC_000014.7:g.23620007del	NCBI36
NG_011697.1:g.8671del
NG_011697.2:g.39062del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.*283del MANE Select	ENSP00000454062.2:n.*283del
ENST00000396997.1:c.*283del	ENSP00000380193.1:n.*283del
ENST00000397002.6:c.*283del	ENSP00000380197.2:n.*283del
ENST00000561028.5:c.*283del	ENSP00000454062.1:n.*283del
NM_006177.3:c.*283del	NP_006168.1:n.*283del
XM_005267708.3:c.*283del	XP_005267765.1:n.*283del
XM_005267709.3:c.*283del	XP_005267766.1:n.*283del
XM_005267710.3:c.*283del	XP_005267767.1:n.*283del
XM_011536801.1:c.*283del	XP_011535103.1:n.*283del
XM_011536802.1:c.*283del	XP_011535104.1:n.*283del
XM_011536803.1:c.*283del	XP_011535105.1:n.*283del
XM_011536804.1:c.*283del	XP_011535106.1:n.*283del
XM_011536805.1:c.*283del	XP_011535107.1:n.*283del
XM_011536806.1:c.*283del	XP_011535108.1:n.*283del
NM_001354768.1:c.*283del	NP_001341697.1:n.*283del
NM_001354769.1:c.*283del	NP_001341698.1:n.*283del
NM_001354770.1:c.*283del	NP_001341699.1:n.*283del
NM_006177.4:c.*283del	NP_006168.1:n.*283del
XM_011536801.2:c.*283del	XP_011535103.2:n.*283del
XM_011536804.2:c.*283del	XP_011535106.1:n.*283del
XM_011536805.2:c.*283del	XP_011535107.1:n.*283del
XM_011536806.2:c.*283del	XP_011535108.2:n.*283del
NM_001354768.3:c.*283del MANE Select	NP_001341697.1:n.*283del
NM_001354770.2:c.*283del	NP_001341699.1:n.*283del
NM_006177.5:c.*283del	NP_006168.1:n.*283del