Canonical Allele Identifier: CA2128327230

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800305C= , CM000676.2:g.33800305C=	GRCh38
NC_000014.8:g.34269511C= , CM000676.1:g.34269511C=	GRCh37
NC_000014.7:g.33339262C=	NCBI36
NG_013036.1:g.866053C=
NG_013036.2:g.866053C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1998C= MANE Select	ENSP00000348460.4:p.Asn666=
ENST00000551634.6:c.2007C=	ENSP00000448373.2:p.Asn669=
ENST00000680362.1:c.1898C=
ENST00000681323.1:c.793+2724C=
ENST00000346562.6:c.1902C=	ENSP00000319610.5:p.Asn634=
ENST00000356141.8:c.1998C=	ENSP00000348460.4:p.Asn666=
ENST00000357798.9:c.1959C=	ENSP00000350446.5:p.Asn653=
ENST00000548645.5:c.1908C=	ENSP00000448916.1:p.Asn636=
ENST00000551492.5:c.2013C=	ENSP00000450392.1:p.Asn671=
ENST00000551634.5:c.1920C=	ENSP00000448373.1:p.Asn640=
NM_001164749.1:c.1998C=	NP_001158221.1:p.Asn666=
NM_001165893.1:c.1908C=	NP_001159365.1:p.Asn636=
NM_022123.2:c.1902C=	NP_071406.1:p.Asn634=
NM_173159.2:c.1959C=	NP_775182.1:p.Asn653=
XM_005267991.2:c.2019C=	XP_005268048.1:p.Asn673=
XM_005267992.2:c.2013C=	XP_005268049.1:p.Asn671=
XM_005267993.2:c.1959C=	XP_005268050.1:p.Asn653=
XM_011537067.1:c.2049C=	XP_011535369.1:p.Asn683=
XM_011537068.1:c.2040C=	XP_011535370.1:p.Asn680=
XM_011537069.1:c.2010C=	XP_011535371.1:p.Asn670=
XM_011537070.1:c.1953C=	XP_011535372.1:p.Asn651=
XM_011537071.1:c.1920C=	XP_011535373.1:p.Asn640=
XM_011537072.1:c.1899C=	XP_011535374.1:p.Asn633=
XM_011537073.1:c.1692C=	XP_011535375.1:p.Asn564=
XM_011537074.1:c.1692C=	XP_011535376.1:p.Asn564=
XM_005267991.3:c.2106C=	XP_005268048.2:p.Asn702=
XM_005267992.3:c.2100C=	XP_005268049.2:p.Asn700=
XM_011537067.2:c.2049C=	XP_011535369.1:p.Asn683=
XM_011537069.2:c.2097C=	XP_011535371.2:p.Asn699=
XM_011537070.2:c.1953C=	XP_011535372.1:p.Asn651=
XM_011537071.2:c.2007C=	XP_011535373.2:p.Asn669=
XM_011537072.2:c.1899C=	XP_011535374.1:p.Asn633=
XM_017021582.1:c.2157C=	XP_016877071.1:p.Asn719=
XM_017021583.1:c.2148C=	XP_016877072.1:p.Asn716=
XM_017021584.1:c.2067C=	XP_016877073.1:p.Asn689=
XM_017021585.1:c.2016C=	XP_016877074.1:p.Asn672=
XM_017021586.1:c.1692C=	XP_016877075.1:p.Asn564=
XM_017021587.1:c.1692C=	XP_016877076.1:p.Asn564=
XM_017021588.1:c.1692C=	XP_016877077.1:p.Asn564=
NM_001164749.2:c.1998C= MANE Select	NP_001158221.1:p.Asn666=
NM_001165893.2:c.1908C=	NP_001159365.1:p.Asn636=
NM_022123.3:c.1902C=	NP_071406.1:p.Asn634=
NM_173159.3:c.1959C=	NP_775182.1:p.Asn653=
NM_001394988.1:c.1953C=	NP_001381917.1:p.Asn651=
NM_001394989.1:c.1899C=	NP_001381918.1:p.Asn633=