Canonical Allele Identifier: CA486093000

Gene: NPAS3

Linked Data

• COSMIC: COSM955419 ; COSM955420 ; COSM1587379
• MyVariant Identifiers: chr14:g.34269487C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800281C>T , CM000676.2:g.33800281C>T	GRCh38
NC_000014.8:g.34269487C>T , CM000676.1:g.34269487C>T	GRCh37
NC_000014.7:g.33339238C>T	NCBI36
NG_013036.1:g.866029C>T
NG_013036.2:g.866029C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1974C>T MANE Select	ENSP00000348460.4:p.Phe658=
ENST00000551634.6:c.1983C>T	ENSP00000448373.2:p.Phe661=
ENST00000680362.1:c.1874C>T
ENST00000681323.1:c.793+2700C>T
ENST00000346562.6:c.1878C>T	ENSP00000319610.5:p.Phe626=
ENST00000356141.8:c.1974C>T	ENSP00000348460.4:p.Phe658=
ENST00000357798.9:c.1935C>T	ENSP00000350446.5:p.Phe645=
ENST00000548645.5:c.1884C>T	ENSP00000448916.1:p.Phe628=
ENST00000551492.5:c.1989C>T	ENSP00000450392.1:p.Phe663=
ENST00000551634.5:c.1896C>T	ENSP00000448373.1:p.Phe632=
NM_001164749.1:c.1974C>T	NP_001158221.1:p.Phe658=
NM_001165893.1:c.1884C>T	NP_001159365.1:p.Phe628=
NM_022123.2:c.1878C>T	NP_071406.1:p.Phe626=
NM_173159.2:c.1935C>T	NP_775182.1:p.Phe645=
XM_005267991.2:c.1995C>T	XP_005268048.1:p.Phe665=
XM_005267992.2:c.1989C>T	XP_005268049.1:p.Phe663=
XM_005267993.2:c.1935C>T	XP_005268050.1:p.Phe645=
XM_011537067.1:c.2025C>T	XP_011535369.1:p.Phe675=
XM_011537068.1:c.2016C>T	XP_011535370.1:p.Phe672=
XM_011537069.1:c.1986C>T	XP_011535371.1:p.Phe662=
XM_011537070.1:c.1929C>T	XP_011535372.1:p.Phe643=
XM_011537071.1:c.1896C>T	XP_011535373.1:p.Phe632=
XM_011537072.1:c.1875C>T	XP_011535374.1:p.Phe625=
XM_011537073.1:c.1668C>T	XP_011535375.1:p.Phe556=
XM_011537074.1:c.1668C>T	XP_011535376.1:p.Phe556=
XM_005267991.3:c.2082C>T	XP_005268048.2:p.Phe694=
XM_005267992.3:c.2076C>T	XP_005268049.2:p.Phe692=
XM_011537067.2:c.2025C>T	XP_011535369.1:p.Phe675=
XM_011537069.2:c.2073C>T	XP_011535371.2:p.Phe691=
XM_011537070.2:c.1929C>T	XP_011535372.1:p.Phe643=
XM_011537071.2:c.1983C>T	XP_011535373.2:p.Phe661=
XM_011537072.2:c.1875C>T	XP_011535374.1:p.Phe625=
XM_017021582.1:c.2133C>T	XP_016877071.1:p.Phe711=
XM_017021583.1:c.2124C>T	XP_016877072.1:p.Phe708=
XM_017021584.1:c.2043C>T	XP_016877073.1:p.Phe681=
XM_017021585.1:c.1992C>T	XP_016877074.1:p.Phe664=
XM_017021586.1:c.1668C>T	XP_016877075.1:p.Phe556=
XM_017021587.1:c.1668C>T	XP_016877076.1:p.Phe556=
XM_017021588.1:c.1668C>T	XP_016877077.1:p.Phe556=
NM_001164749.2:c.1974C>T MANE Select	NP_001158221.1:p.Phe658=
NM_001165893.2:c.1884C>T	NP_001159365.1:p.Phe628=
NM_022123.3:c.1878C>T	NP_071406.1:p.Phe626=
NM_173159.3:c.1935C>T	NP_775182.1:p.Phe645=
NM_001394988.1:c.1929C>T	NP_001381917.1:p.Phe643=
NM_001394989.1:c.1875C>T	NP_001381918.1:p.Phe625=