Canonical Allele Identifier: CA486092837

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269361C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800155C>T , CM000676.2:g.33800155C>T	GRCh38
NC_000014.8:g.34269361C>T , CM000676.1:g.34269361C>T	GRCh37
NC_000014.7:g.33339112C>T	NCBI36
NG_013036.1:g.865903C>T
NG_013036.2:g.865903C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1848C>T MANE Select	ENSP00000348460.4:p.Arg616=
ENST00000551634.6:c.1857C>T	ENSP00000448373.2:p.Arg619=
ENST00000680362.1:c.1748C>T
ENST00000681323.1:c.793+2574C>T
ENST00000346562.6:c.1752C>T	ENSP00000319610.5:p.Arg584=
ENST00000356141.8:c.1848C>T	ENSP00000348460.4:p.Arg616=
ENST00000357798.9:c.1809C>T	ENSP00000350446.5:p.Arg603=
ENST00000548645.5:c.1758C>T	ENSP00000448916.1:p.Arg586=
ENST00000551492.5:c.1863C>T	ENSP00000450392.1:p.Arg621=
ENST00000551634.5:c.1770C>T	ENSP00000448373.1:p.Arg590=
NM_001164749.1:c.1848C>T	NP_001158221.1:p.Arg616=
NM_001165893.1:c.1758C>T	NP_001159365.1:p.Arg586=
NM_022123.2:c.1752C>T	NP_071406.1:p.Arg584=
NM_173159.2:c.1809C>T	NP_775182.1:p.Arg603=
XM_005267991.2:c.1869C>T	XP_005268048.1:p.Arg623=
XM_005267992.2:c.1863C>T	XP_005268049.1:p.Arg621=
XM_005267993.2:c.1809C>T	XP_005268050.1:p.Arg603=
XM_011537067.1:c.1899C>T	XP_011535369.1:p.Arg633=
XM_011537068.1:c.1890C>T	XP_011535370.1:p.Arg630=
XM_011537069.1:c.1860C>T	XP_011535371.1:p.Arg620=
XM_011537070.1:c.1803C>T	XP_011535372.1:p.Arg601=
XM_011537071.1:c.1770C>T	XP_011535373.1:p.Arg590=
XM_011537072.1:c.1749C>T	XP_011535374.1:p.Arg583=
XM_011537073.1:c.1542C>T	XP_011535375.1:p.Arg514=
XM_011537074.1:c.1542C>T	XP_011535376.1:p.Arg514=
XM_005267991.3:c.1956C>T	XP_005268048.2:p.Arg652=
XM_005267992.3:c.1950C>T	XP_005268049.2:p.Arg650=
XM_011537067.2:c.1899C>T	XP_011535369.1:p.Arg633=
XM_011537069.2:c.1947C>T	XP_011535371.2:p.Arg649=
XM_011537070.2:c.1803C>T	XP_011535372.1:p.Arg601=
XM_011537071.2:c.1857C>T	XP_011535373.2:p.Arg619=
XM_011537072.2:c.1749C>T	XP_011535374.1:p.Arg583=
XM_017021582.1:c.2007C>T	XP_016877071.1:p.Arg669=
XM_017021583.1:c.1998C>T	XP_016877072.1:p.Arg666=
XM_017021584.1:c.1917C>T	XP_016877073.1:p.Arg639=
XM_017021585.1:c.1866C>T	XP_016877074.1:p.Arg622=
XM_017021586.1:c.1542C>T	XP_016877075.1:p.Arg514=
XM_017021587.1:c.1542C>T	XP_016877076.1:p.Arg514=
XM_017021588.1:c.1542C>T	XP_016877077.1:p.Arg514=
NM_001164749.2:c.1848C>T MANE Select	NP_001158221.1:p.Arg616=
NM_001165893.2:c.1758C>T	NP_001159365.1:p.Arg586=
NM_022123.3:c.1752C>T	NP_071406.1:p.Arg584=
NM_173159.3:c.1809C>T	NP_775182.1:p.Arg603=
NM_001394988.1:c.1803C>T	NP_001381917.1:p.Arg601=
NM_001394989.1:c.1749C>T	NP_001381918.1:p.Arg583=