Canonical Allele Identifier: CA2128327392

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800402G= , CM000676.2:g.33800402G=	GRCh38
NC_000014.8:g.34269608G= , CM000676.1:g.34269608G=	GRCh37
NC_000014.7:g.33339359G=	NCBI36
NG_013036.1:g.866150G=
NG_013036.2:g.866150G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2095G= MANE Select	ENSP00000348460.4:p.Gly699=
ENST00000551634.6:c.2104G=	ENSP00000448373.2:p.Gly702=
ENST00000680362.1:c.1995G=
ENST00000681323.1:c.793+2821G=
ENST00000346562.6:c.1999G=	ENSP00000319610.5:p.Gly667=
ENST00000356141.8:c.2095G=	ENSP00000348460.4:p.Gly699=
ENST00000357798.9:c.2056G=	ENSP00000350446.5:p.Gly686=
ENST00000548645.5:c.2005G=	ENSP00000448916.1:p.Gly669=
ENST00000551492.5:c.2110G=	ENSP00000450392.1:p.Gly704=
ENST00000551634.5:c.2017G=	ENSP00000448373.1:p.Gly673=
NM_001164749.1:c.2095G=	NP_001158221.1:p.Gly699=
NM_001165893.1:c.2005G=	NP_001159365.1:p.Gly669=
NM_022123.2:c.1999G=	NP_071406.1:p.Gly667=
NM_173159.2:c.2056G=	NP_775182.1:p.Gly686=
XM_005267991.2:c.2116G=	XP_005268048.1:p.Gly706=
XM_005267992.2:c.2110G=	XP_005268049.1:p.Gly704=
XM_005267993.2:c.2056G=	XP_005268050.1:p.Gly686=
XM_011537067.1:c.2146G=	XP_011535369.1:p.Gly716=
XM_011537068.1:c.2137G=	XP_011535370.1:p.Gly713=
XM_011537069.1:c.2107G=	XP_011535371.1:p.Gly703=
XM_011537070.1:c.2050G=	XP_011535372.1:p.Gly684=
XM_011537071.1:c.2017G=	XP_011535373.1:p.Gly673=
XM_011537072.1:c.1996G=	XP_011535374.1:p.Gly666=
XM_011537073.1:c.1789G=	XP_011535375.1:p.Gly597=
XM_011537074.1:c.1789G=	XP_011535376.1:p.Gly597=
XM_005267991.3:c.2203G=	XP_005268048.2:p.Gly735=
XM_005267992.3:c.2197G=	XP_005268049.2:p.Gly733=
XM_011537067.2:c.2146G=	XP_011535369.1:p.Gly716=
XM_011537069.2:c.2194G=	XP_011535371.2:p.Gly732=
XM_011537070.2:c.2050G=	XP_011535372.1:p.Gly684=
XM_011537071.2:c.2104G=	XP_011535373.2:p.Gly702=
XM_011537072.2:c.1996G=	XP_011535374.1:p.Gly666=
XM_017021582.1:c.2254G=	XP_016877071.1:p.Gly752=
XM_017021583.1:c.2245G=	XP_016877072.1:p.Gly749=
XM_017021584.1:c.2164G=	XP_016877073.1:p.Gly722=
XM_017021585.1:c.2113G=	XP_016877074.1:p.Gly705=
XM_017021586.1:c.1789G=	XP_016877075.1:p.Gly597=
XM_017021587.1:c.1789G=	XP_016877076.1:p.Gly597=
XM_017021588.1:c.1789G=	XP_016877077.1:p.Gly597=
NM_001164749.2:c.2095G= MANE Select	NP_001158221.1:p.Gly699=
NM_001165893.2:c.2005G=	NP_001159365.1:p.Gly669=
NM_022123.3:c.1999G=	NP_071406.1:p.Gly667=
NM_173159.3:c.2056G=	NP_775182.1:p.Gly686=
NM_001394988.1:c.2050G=	NP_001381917.1:p.Gly684=
NM_001394989.1:c.1996G=	NP_001381918.1:p.Gly666=