Canonical Allele Identifier: CA389276886

Gene: NRL

Linked Data

• MyVariant Identifiers: chr14:g.24550545A>T (hg19) ; chr14:g.24081336A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24081336A>T , CM000676.2:g.24081336A>T	GRCh38
NC_000014.8:g.24550545A>T , CM000676.1:g.24550545A>T	GRCh37
NC_000014.7:g.23620385A>T	NCBI36
NG_011697.1:g.8288T>A
NG_011697.2:g.38679T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.614T>A MANE Select	ENSP00000454062.2:p.Val205Glu
ENST00000396995.1:c.197T>A	ENSP00000380191.1:p.Val66Glu
ENST00000396997.1:c.614T>A	ENSP00000380193.1:p.Val205Glu
ENST00000397002.6:c.614T>A	ENSP00000380197.2:p.Val205Glu
ENST00000560550.1:c.197T>A	ENSP00000452966.1:p.Val66Glu
ENST00000561028.5:c.614T>A	ENSP00000454062.1:p.Val205Glu
NM_006177.3:c.614T>A	NP_006168.1:p.Val205Glu
XM_005267708.3:c.614T>A	XP_005267765.1:p.Val205Glu
XM_005267709.3:c.614T>A	XP_005267766.1:p.Val205Glu
XM_005267710.3:c.614T>A	XP_005267767.1:p.Val205Glu
XM_011536801.1:c.713T>A	XP_011535103.1:p.Val238Glu
XM_011536802.1:c.614T>A	XP_011535104.1:p.Val205Glu
XM_011536803.1:c.614T>A	XP_011535105.1:p.Val205Glu
XM_011536804.1:c.614T>A	XP_011535106.1:p.Val205Glu
XM_011536805.1:c.614T>A	XP_011535107.1:p.Val205Glu
XM_011536806.1:c.398T>A	XP_011535108.1:p.Val133Glu
NM_001354768.1:c.614T>A	NP_001341697.1:p.Val205Glu
NM_001354769.1:c.614T>A	NP_001341698.1:p.Val205Glu
NM_001354770.1:c.299T>A	NP_001341699.1:p.Val100Glu
NM_006177.4:c.614T>A	NP_006168.1:p.Val205Glu
XM_011536801.2:c.920T>A	XP_011535103.2:p.Val307Glu
XM_011536804.2:c.614T>A	XP_011535106.1:p.Val205Glu
XM_011536805.2:c.614T>A	XP_011535107.1:p.Val205Glu
XM_011536806.2:c.605T>A	XP_011535108.2:p.Val202Glu
NM_001354768.3:c.614T>A MANE Select	NP_001341697.1:p.Val205Glu
NM_001354770.2:c.299T>A	NP_001341699.1:p.Val100Glu
NM_006177.5:c.614T>A	NP_006168.1:p.Val205Glu