Canonical Allele Identifier: CA2128327998

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800574G= , CM000676.2:g.33800574G=	GRCh38
NC_000014.8:g.34269780G= , CM000676.1:g.34269780G=	GRCh37
NC_000014.7:g.33339531G=	NCBI36
NG_013036.1:g.866322G=
NG_013036.2:g.866322G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2267G= MANE Select	ENSP00000348460.4:p.Arg756=
ENST00000551634.6:c.2276G=	ENSP00000448373.2:p.Arg759=
ENST00000680362.1:c.2167G=
ENST00000681323.1:c.793+2993G=
ENST00000346562.6:c.2171G=	ENSP00000319610.5:p.Arg724=
ENST00000356141.8:c.2267G=	ENSP00000348460.4:p.Arg756=
ENST00000357798.9:c.2228G=	ENSP00000350446.5:p.Arg743=
ENST00000548645.5:c.2177G=	ENSP00000448916.1:p.Arg726=
ENST00000551492.5:c.2282G=	ENSP00000450392.1:p.Arg761=
ENST00000551634.5:c.2189G=	ENSP00000448373.1:p.Arg730=
NM_001164749.1:c.2267G=	NP_001158221.1:p.Arg756=
NM_001165893.1:c.2177G=	NP_001159365.1:p.Arg726=
NM_022123.2:c.2171G=	NP_071406.1:p.Arg724=
NM_173159.2:c.2228G=	NP_775182.1:p.Arg743=
XM_005267991.2:c.2288G=	XP_005268048.1:p.Arg763=
XM_005267992.2:c.2282G=	XP_005268049.1:p.Arg761=
XM_005267993.2:c.2228G=	XP_005268050.1:p.Arg743=
XM_011537067.1:c.2318G=	XP_011535369.1:p.Arg773=
XM_011537068.1:c.2309G=	XP_011535370.1:p.Arg770=
XM_011537069.1:c.2279G=	XP_011535371.1:p.Arg760=
XM_011537070.1:c.2222G=	XP_011535372.1:p.Arg741=
XM_011537071.1:c.2189G=	XP_011535373.1:p.Arg730=
XM_011537072.1:c.2168G=	XP_011535374.1:p.Arg723=
XM_011537073.1:c.1961G=	XP_011535375.1:p.Arg654=
XM_011537074.1:c.1961G=	XP_011535376.1:p.Arg654=
XM_005267991.3:c.2375G=	XP_005268048.2:p.Arg792=
XM_005267992.3:c.2369G=	XP_005268049.2:p.Arg790=
XM_011537067.2:c.2318G=	XP_011535369.1:p.Arg773=
XM_011537069.2:c.2366G=	XP_011535371.2:p.Arg789=
XM_011537070.2:c.2222G=	XP_011535372.1:p.Arg741=
XM_011537071.2:c.2276G=	XP_011535373.2:p.Arg759=
XM_011537072.2:c.2168G=	XP_011535374.1:p.Arg723=
XM_017021582.1:c.2426G=	XP_016877071.1:p.Arg809=
XM_017021583.1:c.2417G=	XP_016877072.1:p.Arg806=
XM_017021584.1:c.2336G=	XP_016877073.1:p.Arg779=
XM_017021585.1:c.2285G=	XP_016877074.1:p.Arg762=
XM_017021586.1:c.1961G=	XP_016877075.1:p.Arg654=
XM_017021587.1:c.1961G=	XP_016877076.1:p.Arg654=
XM_017021588.1:c.1961G=	XP_016877077.1:p.Arg654=
NM_001164749.2:c.2267G= MANE Select	NP_001158221.1:p.Arg756=
NM_001165893.2:c.2177G=	NP_001159365.1:p.Arg726=
NM_022123.3:c.2171G=	NP_071406.1:p.Arg724=
NM_173159.3:c.2228G=	NP_775182.1:p.Arg743=
NM_001394988.1:c.2222G=	NP_001381917.1:p.Arg741=
NM_001394989.1:c.2168G=	NP_001381918.1:p.Arg723=