Canonical Allele Identifier: CA2128326838

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800078G= , CM000676.2:g.33800078G=	GRCh38
NC_000014.8:g.34269284G= , CM000676.1:g.34269284G=	GRCh37
NC_000014.7:g.33339035G=	NCBI36
NG_013036.1:g.865826G=
NG_013036.2:g.865826G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1771G= MANE Select	ENSP00000348460.4:p.Ala591=
ENST00000551634.6:c.1780G=	ENSP00000448373.2:p.Ala594=
ENST00000680362.1:c.1671G=
ENST00000681323.1:c.793+2497G=
ENST00000346562.6:c.1675G=	ENSP00000319610.5:p.Ala559=
ENST00000356141.8:c.1771G=	ENSP00000348460.4:p.Ala591=
ENST00000357798.9:c.1732G=	ENSP00000350446.5:p.Ala578=
ENST00000548645.5:c.1681G=	ENSP00000448916.1:p.Ala561=
ENST00000551492.5:c.1786G=	ENSP00000450392.1:p.Ala596=
ENST00000551634.5:c.1693G=	ENSP00000448373.1:p.Ala565=
NM_001164749.1:c.1771G=	NP_001158221.1:p.Ala591=
NM_001165893.1:c.1681G=	NP_001159365.1:p.Ala561=
NM_022123.2:c.1675G=	NP_071406.1:p.Ala559=
NM_173159.2:c.1732G=	NP_775182.1:p.Ala578=
XM_005267991.2:c.1792G=	XP_005268048.1:p.Ala598=
XM_005267992.2:c.1786G=	XP_005268049.1:p.Ala596=
XM_005267993.2:c.1732G=	XP_005268050.1:p.Ala578=
XM_011537067.1:c.1822G=	XP_011535369.1:p.Ala608=
XM_011537068.1:c.1813G=	XP_011535370.1:p.Ala605=
XM_011537069.1:c.1783G=	XP_011535371.1:p.Ala595=
XM_011537070.1:c.1726G=	XP_011535372.1:p.Ala576=
XM_011537071.1:c.1693G=	XP_011535373.1:p.Ala565=
XM_011537072.1:c.1672G=	XP_011535374.1:p.Ala558=
XM_011537073.1:c.1465G=	XP_011535375.1:p.Ala489=
XM_011537074.1:c.1465G=	XP_011535376.1:p.Ala489=
XM_005267991.3:c.1879G=	XP_005268048.2:p.Ala627=
XM_005267992.3:c.1873G=	XP_005268049.2:p.Ala625=
XM_011537067.2:c.1822G=	XP_011535369.1:p.Ala608=
XM_011537069.2:c.1870G=	XP_011535371.2:p.Ala624=
XM_011537070.2:c.1726G=	XP_011535372.1:p.Ala576=
XM_011537071.2:c.1780G=	XP_011535373.2:p.Ala594=
XM_011537072.2:c.1672G=	XP_011535374.1:p.Ala558=
XM_017021582.1:c.1930G=	XP_016877071.1:p.Ala644=
XM_017021583.1:c.1921G=	XP_016877072.1:p.Ala641=
XM_017021584.1:c.1840G=	XP_016877073.1:p.Ala614=
XM_017021585.1:c.1789G=	XP_016877074.1:p.Ala597=
XM_017021586.1:c.1465G=	XP_016877075.1:p.Ala489=
XM_017021587.1:c.1465G=	XP_016877076.1:p.Ala489=
XM_017021588.1:c.1465G=	XP_016877077.1:p.Ala489=
NM_001164749.2:c.1771G= MANE Select	NP_001158221.1:p.Ala591=
NM_001165893.2:c.1681G=	NP_001159365.1:p.Ala561=
NM_022123.3:c.1675G=	NP_071406.1:p.Ala559=
NM_173159.3:c.1732G=	NP_775182.1:p.Ala578=
NM_001394988.1:c.1726G=	NP_001381917.1:p.Ala576=
NM_001394989.1:c.1672G=	NP_001381918.1:p.Ala558=