Canonical Allele Identifier: CA2128327316

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800368C= , CM000676.2:g.33800368C=	GRCh38
NC_000014.8:g.34269574C= , CM000676.1:g.34269574C=	GRCh37
NC_000014.7:g.33339325C=	NCBI36
NG_013036.1:g.866116C=
NG_013036.2:g.866116C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2061C= MANE Select	ENSP00000348460.4:p.Ser687=
ENST00000551634.6:c.2070C=	ENSP00000448373.2:p.Ser690=
ENST00000680362.1:c.1961C=
ENST00000681323.1:c.793+2787C=
ENST00000346562.6:c.1965C=	ENSP00000319610.5:p.Ser655=
ENST00000356141.8:c.2061C=	ENSP00000348460.4:p.Ser687=
ENST00000357798.9:c.2022C=	ENSP00000350446.5:p.Ser674=
ENST00000548645.5:c.1971C=	ENSP00000448916.1:p.Ser657=
ENST00000551492.5:c.2076C=	ENSP00000450392.1:p.Ser692=
ENST00000551634.5:c.1983C=	ENSP00000448373.1:p.Ser661=
NM_001164749.1:c.2061C=	NP_001158221.1:p.Ser687=
NM_001165893.1:c.1971C=	NP_001159365.1:p.Ser657=
NM_022123.2:c.1965C=	NP_071406.1:p.Ser655=
NM_173159.2:c.2022C=	NP_775182.1:p.Ser674=
XM_005267991.2:c.2082C=	XP_005268048.1:p.Ser694=
XM_005267992.2:c.2076C=	XP_005268049.1:p.Ser692=
XM_005267993.2:c.2022C=	XP_005268050.1:p.Ser674=
XM_011537067.1:c.2112C=	XP_011535369.1:p.Ser704=
XM_011537068.1:c.2103C=	XP_011535370.1:p.Ser701=
XM_011537069.1:c.2073C=	XP_011535371.1:p.Ser691=
XM_011537070.1:c.2016C=	XP_011535372.1:p.Ser672=
XM_011537071.1:c.1983C=	XP_011535373.1:p.Ser661=
XM_011537072.1:c.1962C=	XP_011535374.1:p.Ser654=
XM_011537073.1:c.1755C=	XP_011535375.1:p.Ser585=
XM_011537074.1:c.1755C=	XP_011535376.1:p.Ser585=
XM_005267991.3:c.2169C=	XP_005268048.2:p.Ser723=
XM_005267992.3:c.2163C=	XP_005268049.2:p.Ser721=
XM_011537067.2:c.2112C=	XP_011535369.1:p.Ser704=
XM_011537069.2:c.2160C=	XP_011535371.2:p.Ser720=
XM_011537070.2:c.2016C=	XP_011535372.1:p.Ser672=
XM_011537071.2:c.2070C=	XP_011535373.2:p.Ser690=
XM_011537072.2:c.1962C=	XP_011535374.1:p.Ser654=
XM_017021582.1:c.2220C=	XP_016877071.1:p.Ser740=
XM_017021583.1:c.2211C=	XP_016877072.1:p.Ser737=
XM_017021584.1:c.2130C=	XP_016877073.1:p.Ser710=
XM_017021585.1:c.2079C=	XP_016877074.1:p.Ser693=
XM_017021586.1:c.1755C=	XP_016877075.1:p.Ser585=
XM_017021587.1:c.1755C=	XP_016877076.1:p.Ser585=
XM_017021588.1:c.1755C=	XP_016877077.1:p.Ser585=
NM_001164749.2:c.2061C= MANE Select	NP_001158221.1:p.Ser687=
NM_001165893.2:c.1971C=	NP_001159365.1:p.Ser657=
NM_022123.3:c.1965C=	NP_071406.1:p.Ser655=
NM_173159.3:c.2022C=	NP_775182.1:p.Ser674=
NM_001394988.1:c.2016C=	NP_001381917.1:p.Ser672=
NM_001394989.1:c.1962C=	NP_001381918.1:p.Ser654=