Canonical Allele Identifier: CA485775943

Gene: NRL

Linked Data

• MyVariant Identifiers: chr14:g.24550673C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24081464C>T , CM000676.2:g.24081464C>T	GRCh38
NC_000014.8:g.24550673C>T , CM000676.1:g.24550673C>T	GRCh37
NC_000014.7:g.23620513C>T	NCBI36
NG_011697.1:g.8160G>A
NG_011697.2:g.38551G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.486G>A MANE Select	ENSP00000454062.2:p.Gln162=
ENST00000396995.1:c.69G>A	ENSP00000380191.1:p.Gln23=
ENST00000396997.1:c.486G>A	ENSP00000380193.1:p.Gln162=
ENST00000397002.6:c.486G>A	ENSP00000380197.2:p.Gln162=
ENST00000560550.1:c.69G>A	ENSP00000452966.1:p.Gln23=
ENST00000561028.5:c.486G>A	ENSP00000454062.1:p.Gln162=
NM_006177.3:c.486G>A	NP_006168.1:p.Gln162=
XM_005267708.3:c.486G>A	XP_005267765.1:p.Gln162=
XM_005267709.3:c.486G>A	XP_005267766.1:p.Gln162=
XM_005267710.3:c.486G>A	XP_005267767.1:p.Gln162=
XM_011536801.1:c.585G>A	XP_011535103.1:p.Gln195=
XM_011536802.1:c.486G>A	XP_011535104.1:p.Gln162=
XM_011536803.1:c.486G>A	XP_011535105.1:p.Gln162=
XM_011536804.1:c.486G>A	XP_011535106.1:p.Gln162=
XM_011536805.1:c.486G>A	XP_011535107.1:p.Gln162=
XM_011536806.1:c.270G>A	XP_011535108.1:p.Gln90=
NM_001354768.1:c.486G>A	NP_001341697.1:p.Gln162=
NM_001354769.1:c.486G>A	NP_001341698.1:p.Gln162=
NM_001354770.1:c.171G>A	NP_001341699.1:p.Gln57=
NM_006177.4:c.486G>A	NP_006168.1:p.Gln162=
XM_011536801.2:c.792G>A	XP_011535103.2:p.Gln264=
XM_011536804.2:c.486G>A	XP_011535106.1:p.Gln162=
XM_011536805.2:c.486G>A	XP_011535107.1:p.Gln162=
XM_011536806.2:c.477G>A	XP_011535108.2:p.Gln159=
NM_001354768.3:c.486G>A MANE Select	NP_001341697.1:p.Gln162=
NM_001354770.2:c.171G>A	NP_001341699.1:p.Gln57=
NM_006177.5:c.486G>A	NP_006168.1:p.Gln162=