Canonical Allele Identifier: CA2128326912

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800126_33800128delinsCAA , CM000676.2:g.33800126_33800128delinsCAA	GRCh38
NC_000014.8:g.34269332_34269334delinsCAA , CM000676.1:g.34269332_34269334delinsCAA	GRCh37
NC_000014.7:g.33339083_33339085delinsCAA	NCBI36
NG_013036.1:g.865874_865876delinsCAA
NG_013036.2:g.865874_865876delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1819_1821delinsCAA MANE Select	ENSP00000348460.4:p.Gln607=
ENST00000551634.6:c.1828_1830delinsCAA	ENSP00000448373.2:p.Gln610=
ENST00000680362.1:c.1719_1721delinsCAA
ENST00000681323.1:c.793+2545_793+2547delinsCAA
ENST00000346562.6:c.1723_1725delinsCAA	ENSP00000319610.5:p.Gln575=
ENST00000356141.8:c.1819_1821delinsCAA	ENSP00000348460.4:p.Gln607=
ENST00000357798.9:c.1780_1782delinsCAA	ENSP00000350446.5:p.Gln594=
ENST00000548645.5:c.1729_1731delinsCAA	ENSP00000448916.1:p.Gln577=
ENST00000551492.5:c.1834_1836delinsCAA	ENSP00000450392.1:p.Gln612=
ENST00000551634.5:c.1741_1743delinsCAA	ENSP00000448373.1:p.Gln581=
NM_001164749.1:c.1819_1821delinsCAA	NP_001158221.1:p.Gln607=
NM_001165893.1:c.1729_1731delinsCAA	NP_001159365.1:p.Gln577=
NM_022123.2:c.1723_1725delinsCAA	NP_071406.1:p.Gln575=
NM_173159.2:c.1780_1782delinsCAA	NP_775182.1:p.Gln594=
XM_005267991.2:c.1840_1842delinsCAA	XP_005268048.1:p.Gln614=
XM_005267992.2:c.1834_1836delinsCAA	XP_005268049.1:p.Gln612=
XM_005267993.2:c.1780_1782delinsCAA	XP_005268050.1:p.Gln594=
XM_011537067.1:c.1870_1872delinsCAA	XP_011535369.1:p.Gln624=
XM_011537068.1:c.1861_1863delinsCAA	XP_011535370.1:p.Gln621=
XM_011537069.1:c.1831_1833delinsCAA	XP_011535371.1:p.Gln611=
XM_011537070.1:c.1774_1776delinsCAA	XP_011535372.1:p.Gln592=
XM_011537071.1:c.1741_1743delinsCAA	XP_011535373.1:p.Gln581=
XM_011537072.1:c.1720_1722delinsCAA	XP_011535374.1:p.Gln574=
XM_011537073.1:c.1513_1515delinsCAA	XP_011535375.1:p.Gln505=
XM_011537074.1:c.1513_1515delinsCAA	XP_011535376.1:p.Gln505=
XM_005267991.3:c.1927_1929delinsCAA	XP_005268048.2:p.Gln643=
XM_005267992.3:c.1921_1923delinsCAA	XP_005268049.2:p.Gln641=
XM_011537067.2:c.1870_1872delinsCAA	XP_011535369.1:p.Gln624=
XM_011537069.2:c.1918_1920delinsCAA	XP_011535371.2:p.Gln640=
XM_011537070.2:c.1774_1776delinsCAA	XP_011535372.1:p.Gln592=
XM_011537071.2:c.1828_1830delinsCAA	XP_011535373.2:p.Gln610=
XM_011537072.2:c.1720_1722delinsCAA	XP_011535374.1:p.Gln574=
XM_017021582.1:c.1978_1980delinsCAA	XP_016877071.1:p.Gln660=
XM_017021583.1:c.1969_1971delinsCAA	XP_016877072.1:p.Gln657=
XM_017021584.1:c.1888_1890delinsCAA	XP_016877073.1:p.Gln630=
XM_017021585.1:c.1837_1839delinsCAA	XP_016877074.1:p.Gln613=
XM_017021586.1:c.1513_1515delinsCAA	XP_016877075.1:p.Gln505=
XM_017021587.1:c.1513_1515delinsCAA	XP_016877076.1:p.Gln505=
XM_017021588.1:c.1513_1515delinsCAA	XP_016877077.1:p.Gln505=
NM_001164749.2:c.1819_1821delinsCAA MANE Select	NP_001158221.1:p.Gln607=
NM_001165893.2:c.1729_1731delinsCAA	NP_001159365.1:p.Gln577=
NM_022123.3:c.1723_1725delinsCAA	NP_071406.1:p.Gln575=
NM_173159.3:c.1780_1782delinsCAA	NP_775182.1:p.Gln594=
NM_001394988.1:c.1774_1776delinsCAA	NP_001381917.1:p.Gln592=
NM_001394989.1:c.1720_1722delinsCAA	NP_001381918.1:p.Gln574=