Canonical Allele Identifier: CA486093415

Gene: NPAS3

Linked Data

• dbSNP Id: rs10142034
• gnomAD v4: 14-33800569-C-T
• MyVariant Identifiers: chr14:g.34269775C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800569C>T , CM000676.2:g.33800569C>T	GRCh38
NC_000014.8:g.34269775C>T , CM000676.1:g.34269775C>T	GRCh37
NC_000014.7:g.33339526C>T	NCBI36
NG_013036.1:g.866317C>T
NG_013036.2:g.866317C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000356141.9:c.2262C>T MANE Select	ENSP00000348460.4:p.Ser754=
ENST00000551634.6:c.2271C>T	ENSP00000448373.2:p.Ser757=
ENST00000680362.1:c.2162C>T
ENST00000681323.1:c.793+2988C>T
ENST00000346562.6:c.2166C>T	ENSP00000319610.5:p.Ser722=
ENST00000356141.8:c.2262C>T	ENSP00000348460.4:p.Ser754=
ENST00000357798.9:c.2223C>T	ENSP00000350446.5:p.Ser741=
ENST00000548645.5:c.2172C>T	ENSP00000448916.1:p.Ser724=
ENST00000551492.5:c.2277C>T	ENSP00000450392.1:p.Ser759=
ENST00000551634.5:c.2184C>T	ENSP00000448373.1:p.Ser728=
NM_001164749.1:c.2262C>T	NP_001158221.1:p.Ser754=
NM_001165893.1:c.2172C>T	NP_001159365.1:p.Ser724=
NM_022123.2:c.2166C>T	NP_071406.1:p.Ser722=
NM_173159.2:c.2223C>T	NP_775182.1:p.Ser741=
XM_005267991.2:c.2283C>T	XP_005268048.1:p.Ser761=
XM_005267992.2:c.2277C>T	XP_005268049.1:p.Ser759=
XM_005267993.2:c.2223C>T	XP_005268050.1:p.Ser741=
XM_011537067.1:c.2313C>T	XP_011535369.1:p.Ser771=
XM_011537068.1:c.2304C>T	XP_011535370.1:p.Ser768=
XM_011537069.1:c.2274C>T	XP_011535371.1:p.Ser758=
XM_011537070.1:c.2217C>T	XP_011535372.1:p.Ser739=
XM_011537071.1:c.2184C>T	XP_011535373.1:p.Ser728=
XM_011537072.1:c.2163C>T	XP_011535374.1:p.Ser721=
XM_011537073.1:c.1956C>T	XP_011535375.1:p.Ser652=
XM_011537074.1:c.1956C>T	XP_011535376.1:p.Ser652=
XM_005267991.3:c.2370C>T	XP_005268048.2:p.Ser790=
XM_005267992.3:c.2364C>T	XP_005268049.2:p.Ser788=
XM_011537067.2:c.2313C>T	XP_011535369.1:p.Ser771=
XM_011537069.2:c.2361C>T	XP_011535371.2:p.Ser787=
XM_011537070.2:c.2217C>T	XP_011535372.1:p.Ser739=
XM_011537071.2:c.2271C>T	XP_011535373.2:p.Ser757=
XM_011537072.2:c.2163C>T	XP_011535374.1:p.Ser721=
XM_017021582.1:c.2421C>T	XP_016877071.1:p.Ser807=
XM_017021583.1:c.2412C>T	XP_016877072.1:p.Ser804=
XM_017021584.1:c.2331C>T	XP_016877073.1:p.Ser777=
XM_017021585.1:c.2280C>T	XP_016877074.1:p.Ser760=
XM_017021586.1:c.1956C>T	XP_016877075.1:p.Ser652=
XM_017021587.1:c.1956C>T	XP_016877076.1:p.Ser652=
XM_017021588.1:c.1956C>T	XP_016877077.1:p.Ser652=
NM_001164749.2:c.2262C>T MANE Select	NP_001158221.1:p.Ser754=
NM_001165893.2:c.2172C>T	NP_001159365.1:p.Ser724=
NM_022123.3:c.2166C>T	NP_071406.1:p.Ser722=
NM_173159.3:c.2223C>T	NP_775182.1:p.Ser741=
NM_001394988.1:c.2217C>T	NP_001381917.1:p.Ser739=
NM_001394989.1:c.2163C>T	NP_001381918.1:p.Ser721=