Canonical Allele Identifier: CA2128327463

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800424G= , CM000676.2:g.33800424G=	GRCh38
NC_000014.8:g.34269630G= , CM000676.1:g.34269630G=	GRCh37
NC_000014.7:g.33339381G=	NCBI36
NG_013036.1:g.866172G=
NG_013036.2:g.866172G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2117G= MANE Select	ENSP00000348460.4:p.Gly706=
ENST00000551634.6:c.2126G=	ENSP00000448373.2:p.Gly709=
ENST00000680362.1:c.2017G=
ENST00000681323.1:c.793+2843G=
ENST00000346562.6:c.2021G=	ENSP00000319610.5:p.Gly674=
ENST00000356141.8:c.2117G=	ENSP00000348460.4:p.Gly706=
ENST00000357798.9:c.2078G=	ENSP00000350446.5:p.Gly693=
ENST00000548645.5:c.2027G=	ENSP00000448916.1:p.Gly676=
ENST00000551492.5:c.2132G=	ENSP00000450392.1:p.Gly711=
ENST00000551634.5:c.2039G=	ENSP00000448373.1:p.Gly680=
NM_001164749.1:c.2117G=	NP_001158221.1:p.Gly706=
NM_001165893.1:c.2027G=	NP_001159365.1:p.Gly676=
NM_022123.2:c.2021G=	NP_071406.1:p.Gly674=
NM_173159.2:c.2078G=	NP_775182.1:p.Gly693=
XM_005267991.2:c.2138G=	XP_005268048.1:p.Gly713=
XM_005267992.2:c.2132G=	XP_005268049.1:p.Gly711=
XM_005267993.2:c.2078G=	XP_005268050.1:p.Gly693=
XM_011537067.1:c.2168G=	XP_011535369.1:p.Gly723=
XM_011537068.1:c.2159G=	XP_011535370.1:p.Gly720=
XM_011537069.1:c.2129G=	XP_011535371.1:p.Gly710=
XM_011537070.1:c.2072G=	XP_011535372.1:p.Gly691=
XM_011537071.1:c.2039G=	XP_011535373.1:p.Gly680=
XM_011537072.1:c.2018G=	XP_011535374.1:p.Gly673=
XM_011537073.1:c.1811G=	XP_011535375.1:p.Gly604=
XM_011537074.1:c.1811G=	XP_011535376.1:p.Gly604=
XM_005267991.3:c.2225G=	XP_005268048.2:p.Gly742=
XM_005267992.3:c.2219G=	XP_005268049.2:p.Gly740=
XM_011537067.2:c.2168G=	XP_011535369.1:p.Gly723=
XM_011537069.2:c.2216G=	XP_011535371.2:p.Gly739=
XM_011537070.2:c.2072G=	XP_011535372.1:p.Gly691=
XM_011537071.2:c.2126G=	XP_011535373.2:p.Gly709=
XM_011537072.2:c.2018G=	XP_011535374.1:p.Gly673=
XM_017021582.1:c.2276G=	XP_016877071.1:p.Gly759=
XM_017021583.1:c.2267G=	XP_016877072.1:p.Gly756=
XM_017021584.1:c.2186G=	XP_016877073.1:p.Gly729=
XM_017021585.1:c.2135G=	XP_016877074.1:p.Gly712=
XM_017021586.1:c.1811G=	XP_016877075.1:p.Gly604=
XM_017021587.1:c.1811G=	XP_016877076.1:p.Gly604=
XM_017021588.1:c.1811G=	XP_016877077.1:p.Gly604=
NM_001164749.2:c.2117G= MANE Select	NP_001158221.1:p.Gly706=
NM_001165893.2:c.2027G=	NP_001159365.1:p.Gly676=
NM_022123.3:c.2021G=	NP_071406.1:p.Gly674=
NM_173159.3:c.2078G=	NP_775182.1:p.Gly693=
NM_001394988.1:c.2072G=	NP_001381917.1:p.Gly691=
NM_001394989.1:c.2018G=	NP_001381918.1:p.Gly673=