Canonical Allele Identifier: CA389278896

Gene: NRL

Linked Data

• ClinVar Variation Id: 2875470
• ClinVar RCV Id: RCV003707239
• dbSNP Id: rs1477256976
• gnomAD v2: 14-24550746-A-G
• gnomAD v3: 14-24081537-A-G
• gnomAD v4: 14-24081537-A-G
• MyVariant Identifiers: chr14:g.24550746A>G (hg19) ; chr14:g.24081537A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24081537A>G , CM000676.2:g.24081537A>G	GRCh38
NC_000014.8:g.24550746A>G , CM000676.1:g.24550746A>G	GRCh37
NC_000014.7:g.23620586A>G	NCBI36
NG_011697.1:g.8087T>C
NG_011697.2:g.38478T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.413T>C MANE Select	ENSP00000454062.2:p.Val138Ala
ENST00000396995.1:c.-5T>C	ENSP00000380191.1:n.-5T>C
ENST00000396997.1:c.413T>C	ENSP00000380193.1:p.Val138Ala
ENST00000397002.6:c.413T>C	ENSP00000380197.2:p.Val138Ala
ENST00000560550.1:c.-5T>C	ENSP00000452966.1:n.-5T>C
ENST00000561028.5:c.413T>C	ENSP00000454062.1:p.Val138Ala
NM_006177.3:c.413T>C	NP_006168.1:p.Val138Ala
XM_005267708.3:c.413T>C	XP_005267765.1:p.Val138Ala
XM_005267709.3:c.413T>C	XP_005267766.1:p.Val138Ala
XM_005267710.3:c.413T>C	XP_005267767.1:p.Val138Ala
XM_011536801.1:c.512T>C	XP_011535103.1:p.Val171Ala
XM_011536802.1:c.413T>C	XP_011535104.1:p.Val138Ala
XM_011536803.1:c.413T>C	XP_011535105.1:p.Val138Ala
XM_011536804.1:c.413T>C	XP_011535106.1:p.Val138Ala
XM_011536805.1:c.413T>C	XP_011535107.1:p.Val138Ala
XM_011536806.1:c.197T>C	XP_011535108.1:p.Val66Ala
NM_001354768.1:c.413T>C	NP_001341697.1:p.Val138Ala
NM_001354769.1:c.413T>C	NP_001341698.1:p.Val138Ala
NM_001354770.1:c.98T>C	NP_001341699.1:p.Val33Ala
NM_006177.4:c.413T>C	NP_006168.1:p.Val138Ala
XM_011536801.2:c.719T>C	XP_011535103.2:p.Val240Ala
XM_011536804.2:c.413T>C	XP_011535106.1:p.Val138Ala
XM_011536805.2:c.413T>C	XP_011535107.1:p.Val138Ala
XM_011536806.2:c.404T>C	XP_011535108.2:p.Val135Ala
NM_001354768.3:c.413T>C MANE Select	NP_001341697.1:p.Val138Ala
NM_001354770.2:c.98T>C	NP_001341699.1:p.Val33Ala
NM_006177.5:c.413T>C	NP_006168.1:p.Val138Ala