Canonical Allele Identifier: CA2128326777

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800058A= , CM000676.2:g.33800058A=	GRCh38
NC_000014.8:g.34269264A= , CM000676.1:g.34269264A=	GRCh37
NC_000014.7:g.33339015A=	NCBI36
NG_013036.1:g.865806A=
NG_013036.2:g.865806A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1751A= MANE Select	ENSP00000348460.4:p.Asp584=
ENST00000551634.6:c.1760A=	ENSP00000448373.2:p.Asp587=
ENST00000680362.1:c.1651A=
ENST00000681323.1:c.793+2477A=
ENST00000346562.6:c.1655A=	ENSP00000319610.5:p.Asp552=
ENST00000356141.8:c.1751A=	ENSP00000348460.4:p.Asp584=
ENST00000357798.9:c.1712A=	ENSP00000350446.5:p.Asp571=
ENST00000548645.5:c.1661A=	ENSP00000448916.1:p.Asp554=
ENST00000551492.5:c.1766A=	ENSP00000450392.1:p.Asp589=
ENST00000551634.5:c.1673A=	ENSP00000448373.1:p.Asp558=
NM_001164749.1:c.1751A=	NP_001158221.1:p.Asp584=
NM_001165893.1:c.1661A=	NP_001159365.1:p.Asp554=
NM_022123.2:c.1655A=	NP_071406.1:p.Asp552=
NM_173159.2:c.1712A=	NP_775182.1:p.Asp571=
XM_005267991.2:c.1772A=	XP_005268048.1:p.Asp591=
XM_005267992.2:c.1766A=	XP_005268049.1:p.Asp589=
XM_005267993.2:c.1712A=	XP_005268050.1:p.Asp571=
XM_011537067.1:c.1802A=	XP_011535369.1:p.Asp601=
XM_011537068.1:c.1793A=	XP_011535370.1:p.Asp598=
XM_011537069.1:c.1763A=	XP_011535371.1:p.Asp588=
XM_011537070.1:c.1706A=	XP_011535372.1:p.Asp569=
XM_011537071.1:c.1673A=	XP_011535373.1:p.Asp558=
XM_011537072.1:c.1652A=	XP_011535374.1:p.Asp551=
XM_011537073.1:c.1445A=	XP_011535375.1:p.Asp482=
XM_011537074.1:c.1445A=	XP_011535376.1:p.Asp482=
XM_005267991.3:c.1859A=	XP_005268048.2:p.Asp620=
XM_005267992.3:c.1853A=	XP_005268049.2:p.Asp618=
XM_011537067.2:c.1802A=	XP_011535369.1:p.Asp601=
XM_011537069.2:c.1850A=	XP_011535371.2:p.Asp617=
XM_011537070.2:c.1706A=	XP_011535372.1:p.Asp569=
XM_011537071.2:c.1760A=	XP_011535373.2:p.Asp587=
XM_011537072.2:c.1652A=	XP_011535374.1:p.Asp551=
XM_017021582.1:c.1910A=	XP_016877071.1:p.Asp637=
XM_017021583.1:c.1901A=	XP_016877072.1:p.Asp634=
XM_017021584.1:c.1820A=	XP_016877073.1:p.Asp607=
XM_017021585.1:c.1769A=	XP_016877074.1:p.Asp590=
XM_017021586.1:c.1445A=	XP_016877075.1:p.Asp482=
XM_017021587.1:c.1445A=	XP_016877076.1:p.Asp482=
XM_017021588.1:c.1445A=	XP_016877077.1:p.Asp482=
NM_001164749.2:c.1751A= MANE Select	NP_001158221.1:p.Asp584=
NM_001165893.2:c.1661A=	NP_001159365.1:p.Asp554=
NM_022123.3:c.1655A=	NP_071406.1:p.Asp552=
NM_173159.3:c.1712A=	NP_775182.1:p.Asp571=
NM_001394988.1:c.1706A=	NP_001381917.1:p.Asp569=
NM_001394989.1:c.1652A=	NP_001381918.1:p.Asp551=