Canonical Allele Identifier: CA2128327275

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800336G= , CM000676.2:g.33800336G=	GRCh38
NC_000014.8:g.34269542G= , CM000676.1:g.34269542G=	GRCh37
NC_000014.7:g.33339293G=	NCBI36
NG_013036.1:g.866084G=
NG_013036.2:g.866084G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2029G= MANE Select	ENSP00000348460.4:p.Glu677=
ENST00000551634.6:c.2038G=	ENSP00000448373.2:p.Glu680=
ENST00000680362.1:c.1929G=
ENST00000681323.1:c.793+2755G=
ENST00000346562.6:c.1933G=	ENSP00000319610.5:p.Glu645=
ENST00000356141.8:c.2029G=	ENSP00000348460.4:p.Glu677=
ENST00000357798.9:c.1990G=	ENSP00000350446.5:p.Glu664=
ENST00000548645.5:c.1939G=	ENSP00000448916.1:p.Glu647=
ENST00000551492.5:c.2044G=	ENSP00000450392.1:p.Glu682=
ENST00000551634.5:c.1951G=	ENSP00000448373.1:p.Glu651=
NM_001164749.1:c.2029G=	NP_001158221.1:p.Glu677=
NM_001165893.1:c.1939G=	NP_001159365.1:p.Glu647=
NM_022123.2:c.1933G=	NP_071406.1:p.Glu645=
NM_173159.2:c.1990G=	NP_775182.1:p.Glu664=
XM_005267991.2:c.2050G=	XP_005268048.1:p.Glu684=
XM_005267992.2:c.2044G=	XP_005268049.1:p.Glu682=
XM_005267993.2:c.1990G=	XP_005268050.1:p.Glu664=
XM_011537067.1:c.2080G=	XP_011535369.1:p.Glu694=
XM_011537068.1:c.2071G=	XP_011535370.1:p.Glu691=
XM_011537069.1:c.2041G=	XP_011535371.1:p.Glu681=
XM_011537070.1:c.1984G=	XP_011535372.1:p.Glu662=
XM_011537071.1:c.1951G=	XP_011535373.1:p.Glu651=
XM_011537072.1:c.1930G=	XP_011535374.1:p.Glu644=
XM_011537073.1:c.1723G=	XP_011535375.1:p.Glu575=
XM_011537074.1:c.1723G=	XP_011535376.1:p.Glu575=
XM_005267991.3:c.2137G=	XP_005268048.2:p.Glu713=
XM_005267992.3:c.2131G=	XP_005268049.2:p.Glu711=
XM_011537067.2:c.2080G=	XP_011535369.1:p.Glu694=
XM_011537069.2:c.2128G=	XP_011535371.2:p.Glu710=
XM_011537070.2:c.1984G=	XP_011535372.1:p.Glu662=
XM_011537071.2:c.2038G=	XP_011535373.2:p.Glu680=
XM_011537072.2:c.1930G=	XP_011535374.1:p.Glu644=
XM_017021582.1:c.2188G=	XP_016877071.1:p.Glu730=
XM_017021583.1:c.2179G=	XP_016877072.1:p.Glu727=
XM_017021584.1:c.2098G=	XP_016877073.1:p.Glu700=
XM_017021585.1:c.2047G=	XP_016877074.1:p.Glu683=
XM_017021586.1:c.1723G=	XP_016877075.1:p.Glu575=
XM_017021587.1:c.1723G=	XP_016877076.1:p.Glu575=
XM_017021588.1:c.1723G=	XP_016877077.1:p.Glu575=
NM_001164749.2:c.2029G= MANE Select	NP_001158221.1:p.Glu677=
NM_001165893.2:c.1939G=	NP_001159365.1:p.Glu647=
NM_022123.3:c.1933G=	NP_071406.1:p.Glu645=
NM_173159.3:c.1990G=	NP_775182.1:p.Glu664=
NM_001394988.1:c.1984G=	NP_001381917.1:p.Glu662=
NM_001394989.1:c.1930G=	NP_001381918.1:p.Glu644=