Canonical Allele Identifier: CA485775630
Gene: NRL HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.24551890T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24082681T>C , CM000676.2:g.24082681T>C GRCh38
NC_000014.8:g.24551890T>C , CM000676.1:g.24551890T>C GRCh37
NC_000014.7:g.23621730T>C NCBI36
NG_011697.1:g.6943A>G
NG_011697.2:g.37334A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000561028.6:c.168A>G MANE Select ENSP00000454062.2:p.Pro56=
ENST00000396997.1:c.168A>G ENSP00000380193.1:p.Pro56=
ENST00000397002.6:c.168A>G ENSP00000380197.2:p.Pro56=
ENST00000558280.1:c.168A>G ENSP00000454180.1:p.Pro56=
ENST00000561028.5:c.168A>G ENSP00000454062.1:p.Pro56=
NM_006177.3:c.168A>G NP_006168.1:p.Pro56=
XM_005267708.3:c.168A>G XP_005267765.1:p.Pro56=
XM_005267709.3:c.168A>G XP_005267766.1:p.Pro56=
XM_005267710.3:c.168A>G XP_005267767.1:p.Pro56=
XM_011536801.1:c.267A>G XP_011535103.1:p.Pro89=
XM_011536802.1:c.168A>G XP_011535104.1:p.Pro56=
XM_011536803.1:c.168A>G XP_011535105.1:p.Pro56=
XM_011536804.1:c.168A>G XP_011535106.1:p.Pro56=
XM_011536805.1:c.168A>G XP_011535107.1:p.Pro56=
XM_011536806.1:c.165+102A>G XP_011535108.1:n.165+102A>G
NM_001354768.1:c.168A>G NP_001341697.1:p.Pro56=
NM_001354769.1:c.168A>G NP_001341698.1:p.Pro56=
NM_001354770.1:c.66+102A>G NP_001341699.1:n.66+102A>G
NM_006177.4:c.168A>G NP_006168.1:p.Pro56=
XM_011536801.2:c.474A>G XP_011535103.2:p.Pro158=
XM_011536804.2:c.168A>G XP_011535106.1:p.Pro56=
XM_011536805.2:c.168A>G XP_011535107.1:p.Pro56=
XM_011536806.2:c.372+102A>G XP_011535108.2:n.372+102A>G
NM_001354768.3:c.168A>G MANE Select NP_001341697.1:p.Pro56=
NM_001354770.2:c.66+102A>G NP_001341699.1:n.66+102A>G
NM_006177.5:c.168A>G NP_006168.1:p.Pro56=