Canonical Allele Identifier: CA2128327110

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800223C= , CM000676.2:g.33800223C=	GRCh38
NC_000014.8:g.34269429C= , CM000676.1:g.34269429C=	GRCh37
NC_000014.7:g.33339180C=	NCBI36
NG_013036.1:g.865971C=
NG_013036.2:g.865971C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1916C= MANE Select	ENSP00000348460.4:p.Ser639=
ENST00000551634.6:c.1925C=	ENSP00000448373.2:p.Ser642=
ENST00000680362.1:c.1816C=
ENST00000681323.1:c.793+2642C=
ENST00000346562.6:c.1820C=	ENSP00000319610.5:p.Ser607=
ENST00000356141.8:c.1916C=	ENSP00000348460.4:p.Ser639=
ENST00000357798.9:c.1877C=	ENSP00000350446.5:p.Ser626=
ENST00000548645.5:c.1826C=	ENSP00000448916.1:p.Ser609=
ENST00000551492.5:c.1931C=	ENSP00000450392.1:p.Ser644=
ENST00000551634.5:c.1838C=	ENSP00000448373.1:p.Ser613=
NM_001164749.1:c.1916C=	NP_001158221.1:p.Ser639=
NM_001165893.1:c.1826C=	NP_001159365.1:p.Ser609=
NM_022123.2:c.1820C=	NP_071406.1:p.Ser607=
NM_173159.2:c.1877C=	NP_775182.1:p.Ser626=
XM_005267991.2:c.1937C=	XP_005268048.1:p.Ser646=
XM_005267992.2:c.1931C=	XP_005268049.1:p.Ser644=
XM_005267993.2:c.1877C=	XP_005268050.1:p.Ser626=
XM_011537067.1:c.1967C=	XP_011535369.1:p.Ser656=
XM_011537068.1:c.1958C=	XP_011535370.1:p.Ser653=
XM_011537069.1:c.1928C=	XP_011535371.1:p.Ser643=
XM_011537070.1:c.1871C=	XP_011535372.1:p.Ser624=
XM_011537071.1:c.1838C=	XP_011535373.1:p.Ser613=
XM_011537072.1:c.1817C=	XP_011535374.1:p.Ser606=
XM_011537073.1:c.1610C=	XP_011535375.1:p.Ser537=
XM_011537074.1:c.1610C=	XP_011535376.1:p.Ser537=
XM_005267991.3:c.2024C=	XP_005268048.2:p.Ser675=
XM_005267992.3:c.2018C=	XP_005268049.2:p.Ser673=
XM_011537067.2:c.1967C=	XP_011535369.1:p.Ser656=
XM_011537069.2:c.2015C=	XP_011535371.2:p.Ser672=
XM_011537070.2:c.1871C=	XP_011535372.1:p.Ser624=
XM_011537071.2:c.1925C=	XP_011535373.2:p.Ser642=
XM_011537072.2:c.1817C=	XP_011535374.1:p.Ser606=
XM_017021582.1:c.2075C=	XP_016877071.1:p.Ser692=
XM_017021583.1:c.2066C=	XP_016877072.1:p.Ser689=
XM_017021584.1:c.1985C=	XP_016877073.1:p.Ser662=
XM_017021585.1:c.1934C=	XP_016877074.1:p.Ser645=
XM_017021586.1:c.1610C=	XP_016877075.1:p.Ser537=
XM_017021587.1:c.1610C=	XP_016877076.1:p.Ser537=
XM_017021588.1:c.1610C=	XP_016877077.1:p.Ser537=
NM_001164749.2:c.1916C= MANE Select	NP_001158221.1:p.Ser639=
NM_001165893.2:c.1826C=	NP_001159365.1:p.Ser609=
NM_022123.3:c.1820C=	NP_071406.1:p.Ser607=
NM_173159.3:c.1877C=	NP_775182.1:p.Ser626=
NM_001394988.1:c.1871C=	NP_001381917.1:p.Ser624=
NM_001394989.1:c.1817C=	NP_001381918.1:p.Ser606=