Canonical Allele Identifier: CA2128327560

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800465G= , CM000676.2:g.33800465G=	GRCh38
NC_000014.8:g.34269671G= , CM000676.1:g.34269671G=	GRCh37
NC_000014.7:g.33339422G=	NCBI36
NG_013036.1:g.866213G=
NG_013036.2:g.866213G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2158G= MANE Select	ENSP00000348460.4:p.Gly720=
ENST00000551634.6:c.2167G=	ENSP00000448373.2:p.Gly723=
ENST00000680362.1:c.2058G=
ENST00000681323.1:c.793+2884G=
ENST00000346562.6:c.2062G=	ENSP00000319610.5:p.Gly688=
ENST00000356141.8:c.2158G=	ENSP00000348460.4:p.Gly720=
ENST00000357798.9:c.2119G=	ENSP00000350446.5:p.Gly707=
ENST00000548645.5:c.2068G=	ENSP00000448916.1:p.Gly690=
ENST00000551492.5:c.2173G=	ENSP00000450392.1:p.Gly725=
ENST00000551634.5:c.2080G=	ENSP00000448373.1:p.Gly694=
NM_001164749.1:c.2158G=	NP_001158221.1:p.Gly720=
NM_001165893.1:c.2068G=	NP_001159365.1:p.Gly690=
NM_022123.2:c.2062G=	NP_071406.1:p.Gly688=
NM_173159.2:c.2119G=	NP_775182.1:p.Gly707=
XM_005267991.2:c.2179G=	XP_005268048.1:p.Gly727=
XM_005267992.2:c.2173G=	XP_005268049.1:p.Gly725=
XM_005267993.2:c.2119G=	XP_005268050.1:p.Gly707=
XM_011537067.1:c.2209G=	XP_011535369.1:p.Gly737=
XM_011537068.1:c.2200G=	XP_011535370.1:p.Gly734=
XM_011537069.1:c.2170G=	XP_011535371.1:p.Gly724=
XM_011537070.1:c.2113G=	XP_011535372.1:p.Gly705=
XM_011537071.1:c.2080G=	XP_011535373.1:p.Gly694=
XM_011537072.1:c.2059G=	XP_011535374.1:p.Gly687=
XM_011537073.1:c.1852G=	XP_011535375.1:p.Gly618=
XM_011537074.1:c.1852G=	XP_011535376.1:p.Gly618=
XM_005267991.3:c.2266G=	XP_005268048.2:p.Gly756=
XM_005267992.3:c.2260G=	XP_005268049.2:p.Gly754=
XM_011537067.2:c.2209G=	XP_011535369.1:p.Gly737=
XM_011537069.2:c.2257G=	XP_011535371.2:p.Gly753=
XM_011537070.2:c.2113G=	XP_011535372.1:p.Gly705=
XM_011537071.2:c.2167G=	XP_011535373.2:p.Gly723=
XM_011537072.2:c.2059G=	XP_011535374.1:p.Gly687=
XM_017021582.1:c.2317G=	XP_016877071.1:p.Gly773=
XM_017021583.1:c.2308G=	XP_016877072.1:p.Gly770=
XM_017021584.1:c.2227G=	XP_016877073.1:p.Gly743=
XM_017021585.1:c.2176G=	XP_016877074.1:p.Gly726=
XM_017021586.1:c.1852G=	XP_016877075.1:p.Gly618=
XM_017021587.1:c.1852G=	XP_016877076.1:p.Gly618=
XM_017021588.1:c.1852G=	XP_016877077.1:p.Gly618=
NM_001164749.2:c.2158G= MANE Select	NP_001158221.1:p.Gly720=
NM_001165893.2:c.2068G=	NP_001159365.1:p.Gly690=
NM_022123.3:c.2062G=	NP_071406.1:p.Gly688=
NM_173159.3:c.2119G=	NP_775182.1:p.Gly707=
NM_001394988.1:c.2113G=	NP_001381917.1:p.Gly705=
NM_001394989.1:c.2059G=	NP_001381918.1:p.Gly687=