Canonical Allele Identifier: CA2128327192

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800267G= , CM000676.2:g.33800267G=	GRCh38
NC_000014.8:g.34269473G= , CM000676.1:g.34269473G=	GRCh37
NC_000014.7:g.33339224G=	NCBI36
NG_013036.1:g.866015G=
NG_013036.2:g.866015G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1960G= MANE Select	ENSP00000348460.4:p.Glu654=
ENST00000551634.6:c.1969G=	ENSP00000448373.2:p.Glu657=
ENST00000680362.1:c.1860G=
ENST00000681323.1:c.793+2686G=
ENST00000346562.6:c.1864G=	ENSP00000319610.5:p.Glu622=
ENST00000356141.8:c.1960G=	ENSP00000348460.4:p.Glu654=
ENST00000357798.9:c.1921G=	ENSP00000350446.5:p.Glu641=
ENST00000548645.5:c.1870G=	ENSP00000448916.1:p.Glu624=
ENST00000551492.5:c.1975G=	ENSP00000450392.1:p.Glu659=
ENST00000551634.5:c.1882G=	ENSP00000448373.1:p.Glu628=
NM_001164749.1:c.1960G=	NP_001158221.1:p.Glu654=
NM_001165893.1:c.1870G=	NP_001159365.1:p.Glu624=
NM_022123.2:c.1864G=	NP_071406.1:p.Glu622=
NM_173159.2:c.1921G=	NP_775182.1:p.Glu641=
XM_005267991.2:c.1981G=	XP_005268048.1:p.Glu661=
XM_005267992.2:c.1975G=	XP_005268049.1:p.Glu659=
XM_005267993.2:c.1921G=	XP_005268050.1:p.Glu641=
XM_011537067.1:c.2011G=	XP_011535369.1:p.Glu671=
XM_011537068.1:c.2002G=	XP_011535370.1:p.Glu668=
XM_011537069.1:c.1972G=	XP_011535371.1:p.Glu658=
XM_011537070.1:c.1915G=	XP_011535372.1:p.Glu639=
XM_011537071.1:c.1882G=	XP_011535373.1:p.Glu628=
XM_011537072.1:c.1861G=	XP_011535374.1:p.Glu621=
XM_011537073.1:c.1654G=	XP_011535375.1:p.Glu552=
XM_011537074.1:c.1654G=	XP_011535376.1:p.Glu552=
XM_005267991.3:c.2068G=	XP_005268048.2:p.Glu690=
XM_005267992.3:c.2062G=	XP_005268049.2:p.Glu688=
XM_011537067.2:c.2011G=	XP_011535369.1:p.Glu671=
XM_011537069.2:c.2059G=	XP_011535371.2:p.Glu687=
XM_011537070.2:c.1915G=	XP_011535372.1:p.Glu639=
XM_011537071.2:c.1969G=	XP_011535373.2:p.Glu657=
XM_011537072.2:c.1861G=	XP_011535374.1:p.Glu621=
XM_017021582.1:c.2119G=	XP_016877071.1:p.Glu707=
XM_017021583.1:c.2110G=	XP_016877072.1:p.Glu704=
XM_017021584.1:c.2029G=	XP_016877073.1:p.Glu677=
XM_017021585.1:c.1978G=	XP_016877074.1:p.Glu660=
XM_017021586.1:c.1654G=	XP_016877075.1:p.Glu552=
XM_017021587.1:c.1654G=	XP_016877076.1:p.Glu552=
XM_017021588.1:c.1654G=	XP_016877077.1:p.Glu552=
NM_001164749.2:c.1960G= MANE Select	NP_001158221.1:p.Glu654=
NM_001165893.2:c.1870G=	NP_001159365.1:p.Glu624=
NM_022123.3:c.1864G=	NP_071406.1:p.Glu622=
NM_173159.3:c.1921G=	NP_775182.1:p.Glu641=
NM_001394988.1:c.1915G=	NP_001381917.1:p.Glu639=
NM_001394989.1:c.1861G=	NP_001381918.1:p.Glu621=