Canonical Allele Identifier: CA2128327091

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800217T= , CM000676.2:g.33800217T=	GRCh38
NC_000014.8:g.34269423T= , CM000676.1:g.34269423T=	GRCh37
NC_000014.7:g.33339174T=	NCBI36
NG_013036.1:g.865965T=
NG_013036.2:g.865965T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1910T= MANE Select	ENSP00000348460.4:p.Leu637=
ENST00000551634.6:c.1919T=	ENSP00000448373.2:p.Leu640=
ENST00000680362.1:c.1810T=
ENST00000681323.1:c.793+2636T=
ENST00000346562.6:c.1814T=	ENSP00000319610.5:p.Leu605=
ENST00000356141.8:c.1910T=	ENSP00000348460.4:p.Leu637=
ENST00000357798.9:c.1871T=	ENSP00000350446.5:p.Leu624=
ENST00000548645.5:c.1820T=	ENSP00000448916.1:p.Leu607=
ENST00000551492.5:c.1925T=	ENSP00000450392.1:p.Leu642=
ENST00000551634.5:c.1832T=	ENSP00000448373.1:p.Leu611=
NM_001164749.1:c.1910T=	NP_001158221.1:p.Leu637=
NM_001165893.1:c.1820T=	NP_001159365.1:p.Leu607=
NM_022123.2:c.1814T=	NP_071406.1:p.Leu605=
NM_173159.2:c.1871T=	NP_775182.1:p.Leu624=
XM_005267991.2:c.1931T=	XP_005268048.1:p.Leu644=
XM_005267992.2:c.1925T=	XP_005268049.1:p.Leu642=
XM_005267993.2:c.1871T=	XP_005268050.1:p.Leu624=
XM_011537067.1:c.1961T=	XP_011535369.1:p.Leu654=
XM_011537068.1:c.1952T=	XP_011535370.1:p.Leu651=
XM_011537069.1:c.1922T=	XP_011535371.1:p.Leu641=
XM_011537070.1:c.1865T=	XP_011535372.1:p.Leu622=
XM_011537071.1:c.1832T=	XP_011535373.1:p.Leu611=
XM_011537072.1:c.1811T=	XP_011535374.1:p.Leu604=
XM_011537073.1:c.1604T=	XP_011535375.1:p.Leu535=
XM_011537074.1:c.1604T=	XP_011535376.1:p.Leu535=
XM_005267991.3:c.2018T=	XP_005268048.2:p.Leu673=
XM_005267992.3:c.2012T=	XP_005268049.2:p.Leu671=
XM_011537067.2:c.1961T=	XP_011535369.1:p.Leu654=
XM_011537069.2:c.2009T=	XP_011535371.2:p.Leu670=
XM_011537070.2:c.1865T=	XP_011535372.1:p.Leu622=
XM_011537071.2:c.1919T=	XP_011535373.2:p.Leu640=
XM_011537072.2:c.1811T=	XP_011535374.1:p.Leu604=
XM_017021582.1:c.2069T=	XP_016877071.1:p.Leu690=
XM_017021583.1:c.2060T=	XP_016877072.1:p.Leu687=
XM_017021584.1:c.1979T=	XP_016877073.1:p.Leu660=
XM_017021585.1:c.1928T=	XP_016877074.1:p.Leu643=
XM_017021586.1:c.1604T=	XP_016877075.1:p.Leu535=
XM_017021587.1:c.1604T=	XP_016877076.1:p.Leu535=
XM_017021588.1:c.1604T=	XP_016877077.1:p.Leu535=
NM_001164749.2:c.1910T= MANE Select	NP_001158221.1:p.Leu637=
NM_001165893.2:c.1820T=	NP_001159365.1:p.Leu607=
NM_022123.3:c.1814T=	NP_071406.1:p.Leu605=
NM_173159.3:c.1871T=	NP_775182.1:p.Leu624=
NM_001394988.1:c.1865T=	NP_001381917.1:p.Leu622=
NM_001394989.1:c.1811T=	NP_001381918.1:p.Leu604=