Canonical Allele Identifier: CA486092809

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269334A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800128A>G , CM000676.2:g.33800128A>G	GRCh38
NC_000014.8:g.34269334A>G , CM000676.1:g.34269334A>G	GRCh37
NC_000014.7:g.33339085A>G	NCBI36
NG_013036.1:g.865876A>G
NG_013036.2:g.865876A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1821A>G MANE Select	ENSP00000348460.4:p.Gln607=
ENST00000551634.6:c.1830A>G	ENSP00000448373.2:p.Gln610=
ENST00000680362.1:c.1721A>G
ENST00000681323.1:c.793+2547A>G
ENST00000346562.6:c.1725A>G	ENSP00000319610.5:p.Gln575=
ENST00000356141.8:c.1821A>G	ENSP00000348460.4:p.Gln607=
ENST00000357798.9:c.1782A>G	ENSP00000350446.5:p.Gln594=
ENST00000548645.5:c.1731A>G	ENSP00000448916.1:p.Gln577=
ENST00000551492.5:c.1836A>G	ENSP00000450392.1:p.Gln612=
ENST00000551634.5:c.1743A>G	ENSP00000448373.1:p.Gln581=
NM_001164749.1:c.1821A>G	NP_001158221.1:p.Gln607=
NM_001165893.1:c.1731A>G	NP_001159365.1:p.Gln577=
NM_022123.2:c.1725A>G	NP_071406.1:p.Gln575=
NM_173159.2:c.1782A>G	NP_775182.1:p.Gln594=
XM_005267991.2:c.1842A>G	XP_005268048.1:p.Gln614=
XM_005267992.2:c.1836A>G	XP_005268049.1:p.Gln612=
XM_005267993.2:c.1782A>G	XP_005268050.1:p.Gln594=
XM_011537067.1:c.1872A>G	XP_011535369.1:p.Gln624=
XM_011537068.1:c.1863A>G	XP_011535370.1:p.Gln621=
XM_011537069.1:c.1833A>G	XP_011535371.1:p.Gln611=
XM_011537070.1:c.1776A>G	XP_011535372.1:p.Gln592=
XM_011537071.1:c.1743A>G	XP_011535373.1:p.Gln581=
XM_011537072.1:c.1722A>G	XP_011535374.1:p.Gln574=
XM_011537073.1:c.1515A>G	XP_011535375.1:p.Gln505=
XM_011537074.1:c.1515A>G	XP_011535376.1:p.Gln505=
XM_005267991.3:c.1929A>G	XP_005268048.2:p.Gln643=
XM_005267992.3:c.1923A>G	XP_005268049.2:p.Gln641=
XM_011537067.2:c.1872A>G	XP_011535369.1:p.Gln624=
XM_011537069.2:c.1920A>G	XP_011535371.2:p.Gln640=
XM_011537070.2:c.1776A>G	XP_011535372.1:p.Gln592=
XM_011537071.2:c.1830A>G	XP_011535373.2:p.Gln610=
XM_011537072.2:c.1722A>G	XP_011535374.1:p.Gln574=
XM_017021582.1:c.1980A>G	XP_016877071.1:p.Gln660=
XM_017021583.1:c.1971A>G	XP_016877072.1:p.Gln657=
XM_017021584.1:c.1890A>G	XP_016877073.1:p.Gln630=
XM_017021585.1:c.1839A>G	XP_016877074.1:p.Gln613=
XM_017021586.1:c.1515A>G	XP_016877075.1:p.Gln505=
XM_017021587.1:c.1515A>G	XP_016877076.1:p.Gln505=
XM_017021588.1:c.1515A>G	XP_016877077.1:p.Gln505=
NM_001164749.2:c.1821A>G MANE Select	NP_001158221.1:p.Gln607=
NM_001165893.2:c.1731A>G	NP_001159365.1:p.Gln577=
NM_022123.3:c.1725A>G	NP_071406.1:p.Gln575=
NM_173159.3:c.1782A>G	NP_775182.1:p.Gln594=
NM_001394988.1:c.1776A>G	NP_001381917.1:p.Gln592=
NM_001394989.1:c.1722A>G	NP_001381918.1:p.Gln574=