Canonical Allele Identifier: CA2128326953

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800144A= , CM000676.2:g.33800144A=	GRCh38
NC_000014.8:g.34269350A= , CM000676.1:g.34269350A=	GRCh37
NC_000014.7:g.33339101A=	NCBI36
NG_013036.1:g.865892A=
NG_013036.2:g.865892A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1837A= MANE Select	ENSP00000348460.4:p.Ser613=
ENST00000551634.6:c.1846A=	ENSP00000448373.2:p.Ser616=
ENST00000680362.1:c.1737A=
ENST00000681323.1:c.793+2563A=
ENST00000346562.6:c.1741A=	ENSP00000319610.5:p.Ser581=
ENST00000356141.8:c.1837A=	ENSP00000348460.4:p.Ser613=
ENST00000357798.9:c.1798A=	ENSP00000350446.5:p.Ser600=
ENST00000548645.5:c.1747A=	ENSP00000448916.1:p.Ser583=
ENST00000551492.5:c.1852A=	ENSP00000450392.1:p.Ser618=
ENST00000551634.5:c.1759A=	ENSP00000448373.1:p.Ser587=
NM_001164749.1:c.1837A=	NP_001158221.1:p.Ser613=
NM_001165893.1:c.1747A=	NP_001159365.1:p.Ser583=
NM_022123.2:c.1741A=	NP_071406.1:p.Ser581=
NM_173159.2:c.1798A=	NP_775182.1:p.Ser600=
XM_005267991.2:c.1858A=	XP_005268048.1:p.Ser620=
XM_005267992.2:c.1852A=	XP_005268049.1:p.Ser618=
XM_005267993.2:c.1798A=	XP_005268050.1:p.Ser600=
XM_011537067.1:c.1888A=	XP_011535369.1:p.Ser630=
XM_011537068.1:c.1879A=	XP_011535370.1:p.Ser627=
XM_011537069.1:c.1849A=	XP_011535371.1:p.Ser617=
XM_011537070.1:c.1792A=	XP_011535372.1:p.Ser598=
XM_011537071.1:c.1759A=	XP_011535373.1:p.Ser587=
XM_011537072.1:c.1738A=	XP_011535374.1:p.Ser580=
XM_011537073.1:c.1531A=	XP_011535375.1:p.Ser511=
XM_011537074.1:c.1531A=	XP_011535376.1:p.Ser511=
XM_005267991.3:c.1945A=	XP_005268048.2:p.Ser649=
XM_005267992.3:c.1939A=	XP_005268049.2:p.Ser647=
XM_011537067.2:c.1888A=	XP_011535369.1:p.Ser630=
XM_011537069.2:c.1936A=	XP_011535371.2:p.Ser646=
XM_011537070.2:c.1792A=	XP_011535372.1:p.Ser598=
XM_011537071.2:c.1846A=	XP_011535373.2:p.Ser616=
XM_011537072.2:c.1738A=	XP_011535374.1:p.Ser580=
XM_017021582.1:c.1996A=	XP_016877071.1:p.Ser666=
XM_017021583.1:c.1987A=	XP_016877072.1:p.Ser663=
XM_017021584.1:c.1906A=	XP_016877073.1:p.Ser636=
XM_017021585.1:c.1855A=	XP_016877074.1:p.Ser619=
XM_017021586.1:c.1531A=	XP_016877075.1:p.Ser511=
XM_017021587.1:c.1531A=	XP_016877076.1:p.Ser511=
XM_017021588.1:c.1531A=	XP_016877077.1:p.Ser511=
NM_001164749.2:c.1837A= MANE Select	NP_001158221.1:p.Ser613=
NM_001165893.2:c.1747A=	NP_001159365.1:p.Ser583=
NM_022123.3:c.1741A=	NP_071406.1:p.Ser581=
NM_173159.3:c.1798A=	NP_775182.1:p.Ser600=
NM_001394988.1:c.1792A=	NP_001381917.1:p.Ser598=
NM_001394989.1:c.1738A=	NP_001381918.1:p.Ser580=