Canonical Allele Identifier: CA7122919

Gene: NRL

Linked Data

• ClinVar Variation Id: 2010079
• ClinVar RCV Id: RCV002842907
• dbSNP Id: rs754374196
• ExAC: 14:24551931 G / A
• gnomAD v2: 14-24551931-G-A
• gnomAD v3: 14-24082722-G-A
• gnomAD v4: 14-24082722-G-A
• MyVariant Identifiers: chr14:g.24551931G>A (hg19) ; chr14:g.24082722G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24082722G>A , CM000676.2:g.24082722G>A	GRCh38
NC_000014.8:g.24551931G>A , CM000676.1:g.24551931G>A	GRCh37
NC_000014.7:g.23621771G>A	NCBI36
NG_011697.1:g.6902C>T
NG_011697.2:g.37293C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561028.6:c.127C>T MANE Select	ENSP00000454062.2:p.Pro43Ser
ENST00000396997.1:c.127C>T	ENSP00000380193.1:p.Pro43Ser
ENST00000397002.6:c.127C>T	ENSP00000380197.2:p.Pro43Ser
ENST00000558280.1:c.127C>T	ENSP00000454180.1:p.Pro43Ser
ENST00000561028.5:c.127C>T	ENSP00000454062.1:p.Pro43Ser
NM_006177.3:c.127C>T	NP_006168.1:p.Pro43Ser
XM_005267708.3:c.127C>T	XP_005267765.1:p.Pro43Ser
XM_005267709.3:c.127C>T	XP_005267766.1:p.Pro43Ser
XM_005267710.3:c.127C>T	XP_005267767.1:p.Pro43Ser
XM_011536801.1:c.226C>T	XP_011535103.1:p.Pro76Ser
XM_011536802.1:c.127C>T	XP_011535104.1:p.Pro43Ser
XM_011536803.1:c.127C>T	XP_011535105.1:p.Pro43Ser
XM_011536804.1:c.127C>T	XP_011535106.1:p.Pro43Ser
XM_011536805.1:c.127C>T	XP_011535107.1:p.Pro43Ser
XM_011536806.1:c.165+61C>T	XP_011535108.1:n.165+61C>T
NM_001354768.1:c.127C>T	NP_001341697.1:p.Pro43Ser
NM_001354769.1:c.127C>T	NP_001341698.1:p.Pro43Ser
NM_001354770.1:c.66+61C>T	NP_001341699.1:n.66+61C>T
NM_006177.4:c.127C>T	NP_006168.1:p.Pro43Ser
XM_011536801.2:c.433C>T	XP_011535103.2:p.Pro145Ser
XM_011536804.2:c.127C>T	XP_011535106.1:p.Pro43Ser
XM_011536805.2:c.127C>T	XP_011535107.1:p.Pro43Ser
XM_011536806.2:c.372+61C>T	XP_011535108.2:n.372+61C>T
NM_001354768.3:c.127C>T MANE Select	NP_001341697.1:p.Pro43Ser
NM_001354770.2:c.66+61C>T	NP_001341699.1:n.66+61C>T
NM_006177.5:c.127C>T	NP_006168.1:p.Pro43Ser