Canonical Allele Identifier: CA389278705

Gene: NRL

Linked Data

• gnomAD v4: 14-24081517-G-C
• MyVariant Identifiers: chr14:g.24550726G>C (hg19) ; chr14:g.24081517G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24081517G>C , CM000676.2:g.24081517G>C	GRCh38
NC_000014.8:g.24550726G>C , CM000676.1:g.24550726G>C	GRCh37
NC_000014.7:g.23620566G>C	NCBI36
NG_011697.1:g.8107C>G
NG_011697.2:g.38498C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.433C>G MANE Select	ENSP00000454062.2:p.Leu145Val
ENST00000396995.1:c.16C>G	ENSP00000380191.1:p.Leu6Val
ENST00000396997.1:c.433C>G	ENSP00000380193.1:p.Leu145Val
ENST00000397002.6:c.433C>G	ENSP00000380197.2:p.Leu145Val
ENST00000560550.1:c.16C>G	ENSP00000452966.1:p.Leu6Val
ENST00000561028.5:c.433C>G	ENSP00000454062.1:p.Leu145Val
NM_006177.3:c.433C>G	NP_006168.1:p.Leu145Val
XM_005267708.3:c.433C>G	XP_005267765.1:p.Leu145Val
XM_005267709.3:c.433C>G	XP_005267766.1:p.Leu145Val
XM_005267710.3:c.433C>G	XP_005267767.1:p.Leu145Val
XM_011536801.1:c.532C>G	XP_011535103.1:p.Leu178Val
XM_011536802.1:c.433C>G	XP_011535104.1:p.Leu145Val
XM_011536803.1:c.433C>G	XP_011535105.1:p.Leu145Val
XM_011536804.1:c.433C>G	XP_011535106.1:p.Leu145Val
XM_011536805.1:c.433C>G	XP_011535107.1:p.Leu145Val
XM_011536806.1:c.217C>G	XP_011535108.1:p.Leu73Val
NM_001354768.1:c.433C>G	NP_001341697.1:p.Leu145Val
NM_001354769.1:c.433C>G	NP_001341698.1:p.Leu145Val
NM_001354770.1:c.118C>G	NP_001341699.1:p.Leu40Val
NM_006177.4:c.433C>G	NP_006168.1:p.Leu145Val
XM_011536801.2:c.739C>G	XP_011535103.2:p.Leu247Val
XM_011536804.2:c.433C>G	XP_011535106.1:p.Leu145Val
XM_011536805.2:c.433C>G	XP_011535107.1:p.Leu145Val
XM_011536806.2:c.424C>G	XP_011535108.2:p.Leu142Val
NM_001354768.3:c.433C>G MANE Select	NP_001341697.1:p.Leu145Val
NM_001354770.2:c.118C>G	NP_001341699.1:p.Leu40Val
NM_006177.5:c.433C>G	NP_006168.1:p.Leu145Val