Canonical Allele Identifier: CA2128326847

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800083G= , CM000676.2:g.33800083G=	GRCh38
NC_000014.8:g.34269289G= , CM000676.1:g.34269289G=	GRCh37
NC_000014.7:g.33339040G=	NCBI36
NG_013036.1:g.865831G=
NG_013036.2:g.865831G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1776G= MANE Select	ENSP00000348460.4:p.Gln592=
ENST00000551634.6:c.1785G=	ENSP00000448373.2:p.Gln595=
ENST00000680362.1:c.1676G=
ENST00000681323.1:c.793+2502G=
ENST00000346562.6:c.1680G=	ENSP00000319610.5:p.Gln560=
ENST00000356141.8:c.1776G=	ENSP00000348460.4:p.Gln592=
ENST00000357798.9:c.1737G=	ENSP00000350446.5:p.Gln579=
ENST00000548645.5:c.1686G=	ENSP00000448916.1:p.Gln562=
ENST00000551492.5:c.1791G=	ENSP00000450392.1:p.Gln597=
ENST00000551634.5:c.1698G=	ENSP00000448373.1:p.Gln566=
NM_001164749.1:c.1776G=	NP_001158221.1:p.Gln592=
NM_001165893.1:c.1686G=	NP_001159365.1:p.Gln562=
NM_022123.2:c.1680G=	NP_071406.1:p.Gln560=
NM_173159.2:c.1737G=	NP_775182.1:p.Gln579=
XM_005267991.2:c.1797G=	XP_005268048.1:p.Gln599=
XM_005267992.2:c.1791G=	XP_005268049.1:p.Gln597=
XM_005267993.2:c.1737G=	XP_005268050.1:p.Gln579=
XM_011537067.1:c.1827G=	XP_011535369.1:p.Gln609=
XM_011537068.1:c.1818G=	XP_011535370.1:p.Gln606=
XM_011537069.1:c.1788G=	XP_011535371.1:p.Gln596=
XM_011537070.1:c.1731G=	XP_011535372.1:p.Gln577=
XM_011537071.1:c.1698G=	XP_011535373.1:p.Gln566=
XM_011537072.1:c.1677G=	XP_011535374.1:p.Gln559=
XM_011537073.1:c.1470G=	XP_011535375.1:p.Gln490=
XM_011537074.1:c.1470G=	XP_011535376.1:p.Gln490=
XM_005267991.3:c.1884G=	XP_005268048.2:p.Gln628=
XM_005267992.3:c.1878G=	XP_005268049.2:p.Gln626=
XM_011537067.2:c.1827G=	XP_011535369.1:p.Gln609=
XM_011537069.2:c.1875G=	XP_011535371.2:p.Gln625=
XM_011537070.2:c.1731G=	XP_011535372.1:p.Gln577=
XM_011537071.2:c.1785G=	XP_011535373.2:p.Gln595=
XM_011537072.2:c.1677G=	XP_011535374.1:p.Gln559=
XM_017021582.1:c.1935G=	XP_016877071.1:p.Gln645=
XM_017021583.1:c.1926G=	XP_016877072.1:p.Gln642=
XM_017021584.1:c.1845G=	XP_016877073.1:p.Gln615=
XM_017021585.1:c.1794G=	XP_016877074.1:p.Gln598=
XM_017021586.1:c.1470G=	XP_016877075.1:p.Gln490=
XM_017021587.1:c.1470G=	XP_016877076.1:p.Gln490=
XM_017021588.1:c.1470G=	XP_016877077.1:p.Gln490=
NM_001164749.2:c.1776G= MANE Select	NP_001158221.1:p.Gln592=
NM_001165893.2:c.1686G=	NP_001159365.1:p.Gln562=
NM_022123.3:c.1680G=	NP_071406.1:p.Gln560=
NM_173159.3:c.1737G=	NP_775182.1:p.Gln579=
NM_001394988.1:c.1731G=	NP_001381917.1:p.Gln577=
NM_001394989.1:c.1677G=	NP_001381918.1:p.Gln559=