Canonical Allele Identifier: CA2128327332

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800377C= , CM000676.2:g.33800377C=	GRCh38
NC_000014.8:g.34269583C= , CM000676.1:g.34269583C=	GRCh37
NC_000014.7:g.33339334C=	NCBI36
NG_013036.1:g.866125C=
NG_013036.2:g.866125C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2070C= MANE Select	ENSP00000348460.4:p.His690=
ENST00000551634.6:c.2079C=	ENSP00000448373.2:p.His693=
ENST00000680362.1:c.1970C=
ENST00000681323.1:c.793+2796C=
ENST00000346562.6:c.1974C=	ENSP00000319610.5:p.His658=
ENST00000356141.8:c.2070C=	ENSP00000348460.4:p.His690=
ENST00000357798.9:c.2031C=	ENSP00000350446.5:p.His677=
ENST00000548645.5:c.1980C=	ENSP00000448916.1:p.His660=
ENST00000551492.5:c.2085C=	ENSP00000450392.1:p.His695=
ENST00000551634.5:c.1992C=	ENSP00000448373.1:p.His664=
NM_001164749.1:c.2070C=	NP_001158221.1:p.His690=
NM_001165893.1:c.1980C=	NP_001159365.1:p.His660=
NM_022123.2:c.1974C=	NP_071406.1:p.His658=
NM_173159.2:c.2031C=	NP_775182.1:p.His677=
XM_005267991.2:c.2091C=	XP_005268048.1:p.His697=
XM_005267992.2:c.2085C=	XP_005268049.1:p.His695=
XM_005267993.2:c.2031C=	XP_005268050.1:p.His677=
XM_011537067.1:c.2121C=	XP_011535369.1:p.His707=
XM_011537068.1:c.2112C=	XP_011535370.1:p.His704=
XM_011537069.1:c.2082C=	XP_011535371.1:p.His694=
XM_011537070.1:c.2025C=	XP_011535372.1:p.His675=
XM_011537071.1:c.1992C=	XP_011535373.1:p.His664=
XM_011537072.1:c.1971C=	XP_011535374.1:p.His657=
XM_011537073.1:c.1764C=	XP_011535375.1:p.His588=
XM_011537074.1:c.1764C=	XP_011535376.1:p.His588=
XM_005267991.3:c.2178C=	XP_005268048.2:p.His726=
XM_005267992.3:c.2172C=	XP_005268049.2:p.His724=
XM_011537067.2:c.2121C=	XP_011535369.1:p.His707=
XM_011537069.2:c.2169C=	XP_011535371.2:p.His723=
XM_011537070.2:c.2025C=	XP_011535372.1:p.His675=
XM_011537071.2:c.2079C=	XP_011535373.2:p.His693=
XM_011537072.2:c.1971C=	XP_011535374.1:p.His657=
XM_017021582.1:c.2229C=	XP_016877071.1:p.His743=
XM_017021583.1:c.2220C=	XP_016877072.1:p.His740=
XM_017021584.1:c.2139C=	XP_016877073.1:p.His713=
XM_017021585.1:c.2088C=	XP_016877074.1:p.His696=
XM_017021586.1:c.1764C=	XP_016877075.1:p.His588=
XM_017021587.1:c.1764C=	XP_016877076.1:p.His588=
XM_017021588.1:c.1764C=	XP_016877077.1:p.His588=
NM_001164749.2:c.2070C= MANE Select	NP_001158221.1:p.His690=
NM_001165893.2:c.1980C=	NP_001159365.1:p.His660=
NM_022123.3:c.1974C=	NP_071406.1:p.His658=
NM_173159.3:c.2031C=	NP_775182.1:p.His677=
NM_001394988.1:c.2025C=	NP_001381917.1:p.His675=
NM_001394989.1:c.1971C=	NP_001381918.1:p.His657=