Canonical Allele Identifier: CA389412631

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269334A>T (hg19) ; chr14:g.33800128A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1821A>T MANE Select	ENSP00000348460.4:p.Gln607His
ENST00000551634.6:c.1830A>T	ENSP00000448373.2:p.Gln610His
ENST00000680362.1:c.1721A>T
ENST00000681323.1:c.793+2547A>T
ENST00000346562.6:c.1725A>T	ENSP00000319610.5:p.Gln575His
ENST00000356141.8:c.1821A>T	ENSP00000348460.4:p.Gln607His
ENST00000357798.9:c.1782A>T	ENSP00000350446.5:p.Gln594His
ENST00000548645.5:c.1731A>T	ENSP00000448916.1:p.Gln577His
ENST00000551492.5:c.1836A>T	ENSP00000450392.1:p.Gln612His
ENST00000551634.5:c.1743A>T	ENSP00000448373.1:p.Gln581His
NM_001164749.1:c.1821A>T	NP_001158221.1:p.Gln607His
NM_001165893.1:c.1731A>T	NP_001159365.1:p.Gln577His
NM_022123.2:c.1725A>T	NP_071406.1:p.Gln575His
NM_173159.2:c.1782A>T	NP_775182.1:p.Gln594His
XM_005267991.2:c.1842A>T	XP_005268048.1:p.Gln614His
XM_005267992.2:c.1836A>T	XP_005268049.1:p.Gln612His
XM_005267993.2:c.1782A>T	XP_005268050.1:p.Gln594His
XM_011537067.1:c.1872A>T	XP_011535369.1:p.Gln624His
XM_011537068.1:c.1863A>T	XP_011535370.1:p.Gln621His
XM_011537069.1:c.1833A>T	XP_011535371.1:p.Gln611His
XM_011537070.1:c.1776A>T	XP_011535372.1:p.Gln592His
XM_011537071.1:c.1743A>T	XP_011535373.1:p.Gln581His
XM_011537072.1:c.1722A>T	XP_011535374.1:p.Gln574His
XM_011537073.1:c.1515A>T	XP_011535375.1:p.Gln505His
XM_011537074.1:c.1515A>T	XP_011535376.1:p.Gln505His
XM_005267991.3:c.1929A>T	XP_005268048.2:p.Gln643His
XM_005267992.3:c.1923A>T	XP_005268049.2:p.Gln641His
XM_011537067.2:c.1872A>T	XP_011535369.1:p.Gln624His
XM_011537069.2:c.1920A>T	XP_011535371.2:p.Gln640His
XM_011537070.2:c.1776A>T	XP_011535372.1:p.Gln592His
XM_011537071.2:c.1830A>T	XP_011535373.2:p.Gln610His
XM_011537072.2:c.1722A>T	XP_011535374.1:p.Gln574His
XM_017021582.1:c.1980A>T	XP_016877071.1:p.Gln660His
XM_017021583.1:c.1971A>T	XP_016877072.1:p.Gln657His
XM_017021584.1:c.1890A>T	XP_016877073.1:p.Gln630His
XM_017021585.1:c.1839A>T	XP_016877074.1:p.Gln613His
XM_017021586.1:c.1515A>T	XP_016877075.1:p.Gln505His
XM_017021587.1:c.1515A>T	XP_016877076.1:p.Gln505His
XM_017021588.1:c.1515A>T	XP_016877077.1:p.Gln505His
NM_001164749.2:c.1821A>T MANE Select	NP_001158221.1:p.Gln607His
NM_001165893.2:c.1731A>T	NP_001159365.1:p.Gln577His
NM_022123.3:c.1725A>T	NP_071406.1:p.Gln575His
NM_173159.3:c.1782A>T	NP_775182.1:p.Gln594His
NM_001394988.1:c.1776A>T	NP_001381917.1:p.Gln592His
NM_001394989.1:c.1722A>T	NP_001381918.1:p.Gln574His