Canonical Allele Identifier: CA2128326966

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800149C= , CM000676.2:g.33800149C=	GRCh38
NC_000014.8:g.34269355C= , CM000676.1:g.34269355C=	GRCh37
NC_000014.7:g.33339106C=	NCBI36
NG_013036.1:g.865897C=
NG_013036.2:g.865897C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1842C= MANE Select	ENSP00000348460.4:p.Arg614=
ENST00000551634.6:c.1851C=	ENSP00000448373.2:p.Arg617=
ENST00000680362.1:c.1742C=
ENST00000681323.1:c.793+2568C=
ENST00000346562.6:c.1746C=	ENSP00000319610.5:p.Arg582=
ENST00000356141.8:c.1842C=	ENSP00000348460.4:p.Arg614=
ENST00000357798.9:c.1803C=	ENSP00000350446.5:p.Arg601=
ENST00000548645.5:c.1752C=	ENSP00000448916.1:p.Arg584=
ENST00000551492.5:c.1857C=	ENSP00000450392.1:p.Arg619=
ENST00000551634.5:c.1764C=	ENSP00000448373.1:p.Arg588=
NM_001164749.1:c.1842C=	NP_001158221.1:p.Arg614=
NM_001165893.1:c.1752C=	NP_001159365.1:p.Arg584=
NM_022123.2:c.1746C=	NP_071406.1:p.Arg582=
NM_173159.2:c.1803C=	NP_775182.1:p.Arg601=
XM_005267991.2:c.1863C=	XP_005268048.1:p.Arg621=
XM_005267992.2:c.1857C=	XP_005268049.1:p.Arg619=
XM_005267993.2:c.1803C=	XP_005268050.1:p.Arg601=
XM_011537067.1:c.1893C=	XP_011535369.1:p.Arg631=
XM_011537068.1:c.1884C=	XP_011535370.1:p.Arg628=
XM_011537069.1:c.1854C=	XP_011535371.1:p.Arg618=
XM_011537070.1:c.1797C=	XP_011535372.1:p.Arg599=
XM_011537071.1:c.1764C=	XP_011535373.1:p.Arg588=
XM_011537072.1:c.1743C=	XP_011535374.1:p.Arg581=
XM_011537073.1:c.1536C=	XP_011535375.1:p.Arg512=
XM_011537074.1:c.1536C=	XP_011535376.1:p.Arg512=
XM_005267991.3:c.1950C=	XP_005268048.2:p.Arg650=
XM_005267992.3:c.1944C=	XP_005268049.2:p.Arg648=
XM_011537067.2:c.1893C=	XP_011535369.1:p.Arg631=
XM_011537069.2:c.1941C=	XP_011535371.2:p.Arg647=
XM_011537070.2:c.1797C=	XP_011535372.1:p.Arg599=
XM_011537071.2:c.1851C=	XP_011535373.2:p.Arg617=
XM_011537072.2:c.1743C=	XP_011535374.1:p.Arg581=
XM_017021582.1:c.2001C=	XP_016877071.1:p.Arg667=
XM_017021583.1:c.1992C=	XP_016877072.1:p.Arg664=
XM_017021584.1:c.1911C=	XP_016877073.1:p.Arg637=
XM_017021585.1:c.1860C=	XP_016877074.1:p.Arg620=
XM_017021586.1:c.1536C=	XP_016877075.1:p.Arg512=
XM_017021587.1:c.1536C=	XP_016877076.1:p.Arg512=
XM_017021588.1:c.1536C=	XP_016877077.1:p.Arg512=
NM_001164749.2:c.1842C= MANE Select	NP_001158221.1:p.Arg614=
NM_001165893.2:c.1752C=	NP_001159365.1:p.Arg584=
NM_022123.3:c.1746C=	NP_071406.1:p.Arg582=
NM_173159.3:c.1803C=	NP_775182.1:p.Arg601=
NM_001394988.1:c.1797C=	NP_001381917.1:p.Arg599=
NM_001394989.1:c.1743C=	NP_001381918.1:p.Arg581=