Canonical Allele Identifier: CA2128327015

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800175C= , CM000676.2:g.33800175C=	GRCh38
NC_000014.8:g.34269381C= , CM000676.1:g.34269381C=	GRCh37
NC_000014.7:g.33339132C=	NCBI36
NG_013036.1:g.865923C=
NG_013036.2:g.865923C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1868C= MANE Select	ENSP00000348460.4:p.Pro623=
ENST00000551634.6:c.1877C=	ENSP00000448373.2:p.Pro626=
ENST00000680362.1:c.1768C=
ENST00000681323.1:c.793+2594C=
ENST00000346562.6:c.1772C=	ENSP00000319610.5:p.Pro591=
ENST00000356141.8:c.1868C=	ENSP00000348460.4:p.Pro623=
ENST00000357798.9:c.1829C=	ENSP00000350446.5:p.Pro610=
ENST00000548645.5:c.1778C=	ENSP00000448916.1:p.Pro593=
ENST00000551492.5:c.1883C=	ENSP00000450392.1:p.Pro628=
ENST00000551634.5:c.1790C=	ENSP00000448373.1:p.Pro597=
NM_001164749.1:c.1868C=	NP_001158221.1:p.Pro623=
NM_001165893.1:c.1778C=	NP_001159365.1:p.Pro593=
NM_022123.2:c.1772C=	NP_071406.1:p.Pro591=
NM_173159.2:c.1829C=	NP_775182.1:p.Pro610=
XM_005267991.2:c.1889C=	XP_005268048.1:p.Pro630=
XM_005267992.2:c.1883C=	XP_005268049.1:p.Pro628=
XM_005267993.2:c.1829C=	XP_005268050.1:p.Pro610=
XM_011537067.1:c.1919C=	XP_011535369.1:p.Pro640=
XM_011537068.1:c.1910C=	XP_011535370.1:p.Pro637=
XM_011537069.1:c.1880C=	XP_011535371.1:p.Pro627=
XM_011537070.1:c.1823C=	XP_011535372.1:p.Pro608=
XM_011537071.1:c.1790C=	XP_011535373.1:p.Pro597=
XM_011537072.1:c.1769C=	XP_011535374.1:p.Pro590=
XM_011537073.1:c.1562C=	XP_011535375.1:p.Pro521=
XM_011537074.1:c.1562C=	XP_011535376.1:p.Pro521=
XM_005267991.3:c.1976C=	XP_005268048.2:p.Pro659=
XM_005267992.3:c.1970C=	XP_005268049.2:p.Pro657=
XM_011537067.2:c.1919C=	XP_011535369.1:p.Pro640=
XM_011537069.2:c.1967C=	XP_011535371.2:p.Pro656=
XM_011537070.2:c.1823C=	XP_011535372.1:p.Pro608=
XM_011537071.2:c.1877C=	XP_011535373.2:p.Pro626=
XM_011537072.2:c.1769C=	XP_011535374.1:p.Pro590=
XM_017021582.1:c.2027C=	XP_016877071.1:p.Pro676=
XM_017021583.1:c.2018C=	XP_016877072.1:p.Pro673=
XM_017021584.1:c.1937C=	XP_016877073.1:p.Pro646=
XM_017021585.1:c.1886C=	XP_016877074.1:p.Pro629=
XM_017021586.1:c.1562C=	XP_016877075.1:p.Pro521=
XM_017021587.1:c.1562C=	XP_016877076.1:p.Pro521=
XM_017021588.1:c.1562C=	XP_016877077.1:p.Pro521=
NM_001164749.2:c.1868C= MANE Select	NP_001158221.1:p.Pro623=
NM_001165893.2:c.1778C=	NP_001159365.1:p.Pro593=
NM_022123.3:c.1772C=	NP_071406.1:p.Pro591=
NM_173159.3:c.1829C=	NP_775182.1:p.Pro610=
NM_001394988.1:c.1823C=	NP_001381917.1:p.Pro608=
NM_001394989.1:c.1769C=	NP_001381918.1:p.Pro590=