Canonical Allele Identifier: CA389279042

Gene: NRL

Linked Data

• MyVariant Identifiers: chr14:g.24550763A>C (hg19) ; chr14:g.24081554A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24081554A>C , CM000676.2:g.24081554A>C	GRCh38
NC_000014.8:g.24550763A>C , CM000676.1:g.24550763A>C	GRCh37
NC_000014.7:g.23620603A>C	NCBI36
NG_011697.1:g.8070T>G
NG_011697.2:g.38461T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.396T>G MANE Select	ENSP00000454062.2:p.Phe132Leu
ENST00000396995.1:c.-22T>G	ENSP00000380191.1:n.-22T>G
ENST00000396997.1:c.396T>G	ENSP00000380193.1:p.Phe132Leu
ENST00000397002.6:c.396T>G	ENSP00000380197.2:p.Phe132Leu
ENST00000560550.1:c.-22T>G	ENSP00000452966.1:n.-22T>G
ENST00000561028.5:c.396T>G	ENSP00000454062.1:p.Phe132Leu
NM_006177.3:c.396T>G	NP_006168.1:p.Phe132Leu
XM_005267708.3:c.396T>G	XP_005267765.1:p.Phe132Leu
XM_005267709.3:c.396T>G	XP_005267766.1:p.Phe132Leu
XM_005267710.3:c.396T>G	XP_005267767.1:p.Phe132Leu
XM_011536801.1:c.495T>G	XP_011535103.1:p.Phe165Leu
XM_011536802.1:c.396T>G	XP_011535104.1:p.Phe132Leu
XM_011536803.1:c.396T>G	XP_011535105.1:p.Phe132Leu
XM_011536804.1:c.396T>G	XP_011535106.1:p.Phe132Leu
XM_011536805.1:c.396T>G	XP_011535107.1:p.Phe132Leu
XM_011536806.1:c.180T>G	XP_011535108.1:p.Phe60Leu
NM_001354768.1:c.396T>G	NP_001341697.1:p.Phe132Leu
NM_001354769.1:c.396T>G	NP_001341698.1:p.Phe132Leu
NM_001354770.1:c.81T>G	NP_001341699.1:p.Phe27Leu
NM_006177.4:c.396T>G	NP_006168.1:p.Phe132Leu
XM_011536801.2:c.702T>G	XP_011535103.2:p.Phe234Leu
XM_011536804.2:c.396T>G	XP_011535106.1:p.Phe132Leu
XM_011536805.2:c.396T>G	XP_011535107.1:p.Phe132Leu
XM_011536806.2:c.387T>G	XP_011535108.2:p.Phe129Leu
NM_001354768.3:c.396T>G MANE Select	NP_001341697.1:p.Phe132Leu
NM_001354770.2:c.81T>G	NP_001341699.1:p.Phe27Leu
NM_006177.5:c.396T>G	NP_006168.1:p.Phe132Leu