Canonical Allele Identifier: CA2128327214

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800284C= , CM000676.2:g.33800284C=	GRCh38
NC_000014.8:g.34269490C= , CM000676.1:g.34269490C=	GRCh37
NC_000014.7:g.33339241C=	NCBI36
NG_013036.1:g.866032C=
NG_013036.2:g.866032C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1977C= MANE Select	ENSP00000348460.4:p.Asp659=
ENST00000551634.6:c.1986C=	ENSP00000448373.2:p.Asp662=
ENST00000680362.1:c.1877C=
ENST00000681323.1:c.793+2703C=
ENST00000346562.6:c.1881C=	ENSP00000319610.5:p.Asp627=
ENST00000356141.8:c.1977C=	ENSP00000348460.4:p.Asp659=
ENST00000357798.9:c.1938C=	ENSP00000350446.5:p.Asp646=
ENST00000548645.5:c.1887C=	ENSP00000448916.1:p.Asp629=
ENST00000551492.5:c.1992C=	ENSP00000450392.1:p.Asp664=
ENST00000551634.5:c.1899C=	ENSP00000448373.1:p.Asp633=
NM_001164749.1:c.1977C=	NP_001158221.1:p.Asp659=
NM_001165893.1:c.1887C=	NP_001159365.1:p.Asp629=
NM_022123.2:c.1881C=	NP_071406.1:p.Asp627=
NM_173159.2:c.1938C=	NP_775182.1:p.Asp646=
XM_005267991.2:c.1998C=	XP_005268048.1:p.Asp666=
XM_005267992.2:c.1992C=	XP_005268049.1:p.Asp664=
XM_005267993.2:c.1938C=	XP_005268050.1:p.Asp646=
XM_011537067.1:c.2028C=	XP_011535369.1:p.Asp676=
XM_011537068.1:c.2019C=	XP_011535370.1:p.Asp673=
XM_011537069.1:c.1989C=	XP_011535371.1:p.Asp663=
XM_011537070.1:c.1932C=	XP_011535372.1:p.Asp644=
XM_011537071.1:c.1899C=	XP_011535373.1:p.Asp633=
XM_011537072.1:c.1878C=	XP_011535374.1:p.Asp626=
XM_011537073.1:c.1671C=	XP_011535375.1:p.Asp557=
XM_011537074.1:c.1671C=	XP_011535376.1:p.Asp557=
XM_005267991.3:c.2085C=	XP_005268048.2:p.Asp695=
XM_005267992.3:c.2079C=	XP_005268049.2:p.Asp693=
XM_011537067.2:c.2028C=	XP_011535369.1:p.Asp676=
XM_011537069.2:c.2076C=	XP_011535371.2:p.Asp692=
XM_011537070.2:c.1932C=	XP_011535372.1:p.Asp644=
XM_011537071.2:c.1986C=	XP_011535373.2:p.Asp662=
XM_011537072.2:c.1878C=	XP_011535374.1:p.Asp626=
XM_017021582.1:c.2136C=	XP_016877071.1:p.Asp712=
XM_017021583.1:c.2127C=	XP_016877072.1:p.Asp709=
XM_017021584.1:c.2046C=	XP_016877073.1:p.Asp682=
XM_017021585.1:c.1995C=	XP_016877074.1:p.Asp665=
XM_017021586.1:c.1671C=	XP_016877075.1:p.Asp557=
XM_017021587.1:c.1671C=	XP_016877076.1:p.Asp557=
XM_017021588.1:c.1671C=	XP_016877077.1:p.Asp557=
NM_001164749.2:c.1977C= MANE Select	NP_001158221.1:p.Asp659=
NM_001165893.2:c.1887C=	NP_001159365.1:p.Asp629=
NM_022123.3:c.1881C=	NP_071406.1:p.Asp627=
NM_173159.3:c.1938C=	NP_775182.1:p.Asp646=
NM_001394988.1:c.1932C=	NP_001381917.1:p.Asp644=
NM_001394989.1:c.1878C=	NP_001381918.1:p.Asp626=