Canonical Allele Identifier: CA389278669

Gene: NRL

Linked Data

• MyVariant Identifiers: chr14:g.24550722T>G (hg19) ; chr14:g.24081513T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24081513T>G , CM000676.2:g.24081513T>G	GRCh38
NC_000014.8:g.24550722T>G , CM000676.1:g.24550722T>G	GRCh37
NC_000014.7:g.23620562T>G	NCBI36
NG_011697.1:g.8111A>C
NG_011697.2:g.38502A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.437A>C MANE Select	ENSP00000454062.2:p.Asn146Thr
ENST00000396995.1:c.20A>C	ENSP00000380191.1:p.Asn7Thr
ENST00000396997.1:c.437A>C	ENSP00000380193.1:p.Asn146Thr
ENST00000397002.6:c.437A>C	ENSP00000380197.2:p.Asn146Thr
ENST00000560550.1:c.20A>C	ENSP00000452966.1:p.Asn7Thr
ENST00000561028.5:c.437A>C	ENSP00000454062.1:p.Asn146Thr
NM_006177.3:c.437A>C	NP_006168.1:p.Asn146Thr
XM_005267708.3:c.437A>C	XP_005267765.1:p.Asn146Thr
XM_005267709.3:c.437A>C	XP_005267766.1:p.Asn146Thr
XM_005267710.3:c.437A>C	XP_005267767.1:p.Asn146Thr
XM_011536801.1:c.536A>C	XP_011535103.1:p.Asn179Thr
XM_011536802.1:c.437A>C	XP_011535104.1:p.Asn146Thr
XM_011536803.1:c.437A>C	XP_011535105.1:p.Asn146Thr
XM_011536804.1:c.437A>C	XP_011535106.1:p.Asn146Thr
XM_011536805.1:c.437A>C	XP_011535107.1:p.Asn146Thr
XM_011536806.1:c.221A>C	XP_011535108.1:p.Asn74Thr
NM_001354768.1:c.437A>C	NP_001341697.1:p.Asn146Thr
NM_001354769.1:c.437A>C	NP_001341698.1:p.Asn146Thr
NM_001354770.1:c.122A>C	NP_001341699.1:p.Asn41Thr
NM_006177.4:c.437A>C	NP_006168.1:p.Asn146Thr
XM_011536801.2:c.743A>C	XP_011535103.2:p.Asn248Thr
XM_011536804.2:c.437A>C	XP_011535106.1:p.Asn146Thr
XM_011536805.2:c.437A>C	XP_011535107.1:p.Asn146Thr
XM_011536806.2:c.428A>C	XP_011535108.2:p.Asn143Thr
NM_001354768.3:c.437A>C MANE Select	NP_001341697.1:p.Asn146Thr
NM_001354770.2:c.122A>C	NP_001341699.1:p.Asn41Thr
NM_006177.5:c.437A>C	NP_006168.1:p.Asn146Thr