Canonical Allele Identifier: CA485775737

Gene: NRL

Linked Data

• MyVariant Identifiers: chr14:g.24550586G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24081377G>C , CM000676.2:g.24081377G>C	GRCh38
NC_000014.8:g.24550586G>C , CM000676.1:g.24550586G>C	GRCh37
NC_000014.7:g.23620426G>C	NCBI36
NG_011697.1:g.8247C>G
NG_011697.2:g.38638C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.573C>G MANE Select	ENSP00000454062.2:p.Arg191=
ENST00000396995.1:c.156C>G	ENSP00000380191.1:p.Arg52=
ENST00000396997.1:c.573C>G	ENSP00000380193.1:p.Arg191=
ENST00000397002.6:c.573C>G	ENSP00000380197.2:p.Arg191=
ENST00000560550.1:c.156C>G	ENSP00000452966.1:p.Arg52=
ENST00000561028.5:c.573C>G	ENSP00000454062.1:p.Arg191=
NM_006177.3:c.573C>G	NP_006168.1:p.Arg191=
XM_005267708.3:c.573C>G	XP_005267765.1:p.Arg191=
XM_005267709.3:c.573C>G	XP_005267766.1:p.Arg191=
XM_005267710.3:c.573C>G	XP_005267767.1:p.Arg191=
XM_011536801.1:c.672C>G	XP_011535103.1:p.Arg224=
XM_011536802.1:c.573C>G	XP_011535104.1:p.Arg191=
XM_011536803.1:c.573C>G	XP_011535105.1:p.Arg191=
XM_011536804.1:c.573C>G	XP_011535106.1:p.Arg191=
XM_011536805.1:c.573C>G	XP_011535107.1:p.Arg191=
XM_011536806.1:c.357C>G	XP_011535108.1:p.Arg119=
NM_001354768.1:c.573C>G	NP_001341697.1:p.Arg191=
NM_001354769.1:c.573C>G	NP_001341698.1:p.Arg191=
NM_001354770.1:c.258C>G	NP_001341699.1:p.Arg86=
NM_006177.4:c.573C>G	NP_006168.1:p.Arg191=
XM_011536801.2:c.879C>G	XP_011535103.2:p.Arg293=
XM_011536804.2:c.573C>G	XP_011535106.1:p.Arg191=
XM_011536805.2:c.573C>G	XP_011535107.1:p.Arg191=
XM_011536806.2:c.564C>G	XP_011535108.2:p.Arg188=
NM_001354768.3:c.573C>G MANE Select	NP_001341697.1:p.Arg191=
NM_001354770.2:c.258C>G	NP_001341699.1:p.Arg86=
NM_006177.5:c.573C>G	NP_006168.1:p.Arg191=