Canonical Allele Identifier: CA2128326963

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800148G= , CM000676.2:g.33800148G=	GRCh38
NC_000014.8:g.34269354G= , CM000676.1:g.34269354G=	GRCh37
NC_000014.7:g.33339105G=	NCBI36
NG_013036.1:g.865896G=
NG_013036.2:g.865896G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1841G= MANE Select	ENSP00000348460.4:p.Arg614=
ENST00000551634.6:c.1850G=	ENSP00000448373.2:p.Arg617=
ENST00000680362.1:c.1741G=
ENST00000681323.1:c.793+2567G=
ENST00000346562.6:c.1745G=	ENSP00000319610.5:p.Arg582=
ENST00000356141.8:c.1841G=	ENSP00000348460.4:p.Arg614=
ENST00000357798.9:c.1802G=	ENSP00000350446.5:p.Arg601=
ENST00000548645.5:c.1751G=	ENSP00000448916.1:p.Arg584=
ENST00000551492.5:c.1856G=	ENSP00000450392.1:p.Arg619=
ENST00000551634.5:c.1763G=	ENSP00000448373.1:p.Arg588=
NM_001164749.1:c.1841G=	NP_001158221.1:p.Arg614=
NM_001165893.1:c.1751G=	NP_001159365.1:p.Arg584=
NM_022123.2:c.1745G=	NP_071406.1:p.Arg582=
NM_173159.2:c.1802G=	NP_775182.1:p.Arg601=
XM_005267991.2:c.1862G=	XP_005268048.1:p.Arg621=
XM_005267992.2:c.1856G=	XP_005268049.1:p.Arg619=
XM_005267993.2:c.1802G=	XP_005268050.1:p.Arg601=
XM_011537067.1:c.1892G=	XP_011535369.1:p.Arg631=
XM_011537068.1:c.1883G=	XP_011535370.1:p.Arg628=
XM_011537069.1:c.1853G=	XP_011535371.1:p.Arg618=
XM_011537070.1:c.1796G=	XP_011535372.1:p.Arg599=
XM_011537071.1:c.1763G=	XP_011535373.1:p.Arg588=
XM_011537072.1:c.1742G=	XP_011535374.1:p.Arg581=
XM_011537073.1:c.1535G=	XP_011535375.1:p.Arg512=
XM_011537074.1:c.1535G=	XP_011535376.1:p.Arg512=
XM_005267991.3:c.1949G=	XP_005268048.2:p.Arg650=
XM_005267992.3:c.1943G=	XP_005268049.2:p.Arg648=
XM_011537067.2:c.1892G=	XP_011535369.1:p.Arg631=
XM_011537069.2:c.1940G=	XP_011535371.2:p.Arg647=
XM_011537070.2:c.1796G=	XP_011535372.1:p.Arg599=
XM_011537071.2:c.1850G=	XP_011535373.2:p.Arg617=
XM_011537072.2:c.1742G=	XP_011535374.1:p.Arg581=
XM_017021582.1:c.2000G=	XP_016877071.1:p.Arg667=
XM_017021583.1:c.1991G=	XP_016877072.1:p.Arg664=
XM_017021584.1:c.1910G=	XP_016877073.1:p.Arg637=
XM_017021585.1:c.1859G=	XP_016877074.1:p.Arg620=
XM_017021586.1:c.1535G=	XP_016877075.1:p.Arg512=
XM_017021587.1:c.1535G=	XP_016877076.1:p.Arg512=
XM_017021588.1:c.1535G=	XP_016877077.1:p.Arg512=
NM_001164749.2:c.1841G= MANE Select	NP_001158221.1:p.Arg614=
NM_001165893.2:c.1751G=	NP_001159365.1:p.Arg584=
NM_022123.3:c.1745G=	NP_071406.1:p.Arg582=
NM_173159.3:c.1802G=	NP_775182.1:p.Arg601=
NM_001394988.1:c.1796G=	NP_001381917.1:p.Arg599=
NM_001394989.1:c.1742G=	NP_001381918.1:p.Arg581=