Canonical Allele Identifier: CA389278952

Gene: NRL

Linked Data

• MyVariant Identifiers: chr14:g.24550750G>T (hg19) ; chr14:g.24081541G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24081541G>T , CM000676.2:g.24081541G>T	GRCh38
NC_000014.8:g.24550750G>T , CM000676.1:g.24550750G>T	GRCh37
NC_000014.7:g.23620590G>T	NCBI36
NG_011697.1:g.8083C>A
NG_011697.2:g.38474C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.409C>A MANE Select	ENSP00000454062.2:p.Leu137Met
ENST00000396995.1:c.-9C>A	ENSP00000380191.1:n.-9C>A
ENST00000396997.1:c.409C>A	ENSP00000380193.1:p.Leu137Met
ENST00000397002.6:c.409C>A	ENSP00000380197.2:p.Leu137Met
ENST00000560550.1:c.-9C>A	ENSP00000452966.1:n.-9C>A
ENST00000561028.5:c.409C>A	ENSP00000454062.1:p.Leu137Met
NM_006177.3:c.409C>A	NP_006168.1:p.Leu137Met
XM_005267708.3:c.409C>A	XP_005267765.1:p.Leu137Met
XM_005267709.3:c.409C>A	XP_005267766.1:p.Leu137Met
XM_005267710.3:c.409C>A	XP_005267767.1:p.Leu137Met
XM_011536801.1:c.508C>A	XP_011535103.1:p.Leu170Met
XM_011536802.1:c.409C>A	XP_011535104.1:p.Leu137Met
XM_011536803.1:c.409C>A	XP_011535105.1:p.Leu137Met
XM_011536804.1:c.409C>A	XP_011535106.1:p.Leu137Met
XM_011536805.1:c.409C>A	XP_011535107.1:p.Leu137Met
XM_011536806.1:c.193C>A	XP_011535108.1:p.Leu65Met
NM_001354768.1:c.409C>A	NP_001341697.1:p.Leu137Met
NM_001354769.1:c.409C>A	NP_001341698.1:p.Leu137Met
NM_001354770.1:c.94C>A	NP_001341699.1:p.Leu32Met
NM_006177.4:c.409C>A	NP_006168.1:p.Leu137Met
XM_011536801.2:c.715C>A	XP_011535103.2:p.Leu239Met
XM_011536804.2:c.409C>A	XP_011535106.1:p.Leu137Met
XM_011536805.2:c.409C>A	XP_011535107.1:p.Leu137Met
XM_011536806.2:c.400C>A	XP_011535108.2:p.Leu134Met
NM_001354768.3:c.409C>A MANE Select	NP_001341697.1:p.Leu137Met
NM_001354770.2:c.94C>A	NP_001341699.1:p.Leu32Met
NM_006177.5:c.409C>A	NP_006168.1:p.Leu137Met