Canonical Allele Identifier: CA2128327134

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800236C= , CM000676.2:g.33800236C=	GRCh38
NC_000014.8:g.34269442C= , CM000676.1:g.34269442C=	GRCh37
NC_000014.7:g.33339193C=	NCBI36
NG_013036.1:g.865984C=
NG_013036.2:g.865984C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1929C= MANE Select	ENSP00000348460.4:p.Ala643=
ENST00000551634.6:c.1938C=	ENSP00000448373.2:p.Ala646=
ENST00000680362.1:c.1829C=
ENST00000681323.1:c.793+2655C=
ENST00000346562.6:c.1833C=	ENSP00000319610.5:p.Ala611=
ENST00000356141.8:c.1929C=	ENSP00000348460.4:p.Ala643=
ENST00000357798.9:c.1890C=	ENSP00000350446.5:p.Ala630=
ENST00000548645.5:c.1839C=	ENSP00000448916.1:p.Ala613=
ENST00000551492.5:c.1944C=	ENSP00000450392.1:p.Ala648=
ENST00000551634.5:c.1851C=	ENSP00000448373.1:p.Ala617=
NM_001164749.1:c.1929C=	NP_001158221.1:p.Ala643=
NM_001165893.1:c.1839C=	NP_001159365.1:p.Ala613=
NM_022123.2:c.1833C=	NP_071406.1:p.Ala611=
NM_173159.2:c.1890C=	NP_775182.1:p.Ala630=
XM_005267991.2:c.1950C=	XP_005268048.1:p.Ala650=
XM_005267992.2:c.1944C=	XP_005268049.1:p.Ala648=
XM_005267993.2:c.1890C=	XP_005268050.1:p.Ala630=
XM_011537067.1:c.1980C=	XP_011535369.1:p.Ala660=
XM_011537068.1:c.1971C=	XP_011535370.1:p.Ala657=
XM_011537069.1:c.1941C=	XP_011535371.1:p.Ala647=
XM_011537070.1:c.1884C=	XP_011535372.1:p.Ala628=
XM_011537071.1:c.1851C=	XP_011535373.1:p.Ala617=
XM_011537072.1:c.1830C=	XP_011535374.1:p.Ala610=
XM_011537073.1:c.1623C=	XP_011535375.1:p.Ala541=
XM_011537074.1:c.1623C=	XP_011535376.1:p.Ala541=
XM_005267991.3:c.2037C=	XP_005268048.2:p.Ala679=
XM_005267992.3:c.2031C=	XP_005268049.2:p.Ala677=
XM_011537067.2:c.1980C=	XP_011535369.1:p.Ala660=
XM_011537069.2:c.2028C=	XP_011535371.2:p.Ala676=
XM_011537070.2:c.1884C=	XP_011535372.1:p.Ala628=
XM_011537071.2:c.1938C=	XP_011535373.2:p.Ala646=
XM_011537072.2:c.1830C=	XP_011535374.1:p.Ala610=
XM_017021582.1:c.2088C=	XP_016877071.1:p.Ala696=
XM_017021583.1:c.2079C=	XP_016877072.1:p.Ala693=
XM_017021584.1:c.1998C=	XP_016877073.1:p.Ala666=
XM_017021585.1:c.1947C=	XP_016877074.1:p.Ala649=
XM_017021586.1:c.1623C=	XP_016877075.1:p.Ala541=
XM_017021587.1:c.1623C=	XP_016877076.1:p.Ala541=
XM_017021588.1:c.1623C=	XP_016877077.1:p.Ala541=
NM_001164749.2:c.1929C= MANE Select	NP_001158221.1:p.Ala643=
NM_001165893.2:c.1839C=	NP_001159365.1:p.Ala613=
NM_022123.3:c.1833C=	NP_071406.1:p.Ala611=
NM_173159.3:c.1890C=	NP_775182.1:p.Ala630=
NM_001394988.1:c.1884C=	NP_001381917.1:p.Ala628=
NM_001394989.1:c.1830C=	NP_001381918.1:p.Ala610=