Canonical Allele Identifier: CA486092827

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269352C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800146C>T , CM000676.2:g.33800146C>T	GRCh38
NC_000014.8:g.34269352C>T , CM000676.1:g.34269352C>T	GRCh37
NC_000014.7:g.33339103C>T	NCBI36
NG_013036.1:g.865894C>T
NG_013036.2:g.865894C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1839C>T MANE Select	ENSP00000348460.4:p.Ser613=
ENST00000551634.6:c.1848C>T	ENSP00000448373.2:p.Ser616=
ENST00000680362.1:c.1739C>T
ENST00000681323.1:c.793+2565C>T
ENST00000346562.6:c.1743C>T	ENSP00000319610.5:p.Ser581=
ENST00000356141.8:c.1839C>T	ENSP00000348460.4:p.Ser613=
ENST00000357798.9:c.1800C>T	ENSP00000350446.5:p.Ser600=
ENST00000548645.5:c.1749C>T	ENSP00000448916.1:p.Ser583=
ENST00000551492.5:c.1854C>T	ENSP00000450392.1:p.Ser618=
ENST00000551634.5:c.1761C>T	ENSP00000448373.1:p.Ser587=
NM_001164749.1:c.1839C>T	NP_001158221.1:p.Ser613=
NM_001165893.1:c.1749C>T	NP_001159365.1:p.Ser583=
NM_022123.2:c.1743C>T	NP_071406.1:p.Ser581=
NM_173159.2:c.1800C>T	NP_775182.1:p.Ser600=
XM_005267991.2:c.1860C>T	XP_005268048.1:p.Ser620=
XM_005267992.2:c.1854C>T	XP_005268049.1:p.Ser618=
XM_005267993.2:c.1800C>T	XP_005268050.1:p.Ser600=
XM_011537067.1:c.1890C>T	XP_011535369.1:p.Ser630=
XM_011537068.1:c.1881C>T	XP_011535370.1:p.Ser627=
XM_011537069.1:c.1851C>T	XP_011535371.1:p.Ser617=
XM_011537070.1:c.1794C>T	XP_011535372.1:p.Ser598=
XM_011537071.1:c.1761C>T	XP_011535373.1:p.Ser587=
XM_011537072.1:c.1740C>T	XP_011535374.1:p.Ser580=
XM_011537073.1:c.1533C>T	XP_011535375.1:p.Ser511=
XM_011537074.1:c.1533C>T	XP_011535376.1:p.Ser511=
XM_005267991.3:c.1947C>T	XP_005268048.2:p.Ser649=
XM_005267992.3:c.1941C>T	XP_005268049.2:p.Ser647=
XM_011537067.2:c.1890C>T	XP_011535369.1:p.Ser630=
XM_011537069.2:c.1938C>T	XP_011535371.2:p.Ser646=
XM_011537070.2:c.1794C>T	XP_011535372.1:p.Ser598=
XM_011537071.2:c.1848C>T	XP_011535373.2:p.Ser616=
XM_011537072.2:c.1740C>T	XP_011535374.1:p.Ser580=
XM_017021582.1:c.1998C>T	XP_016877071.1:p.Ser666=
XM_017021583.1:c.1989C>T	XP_016877072.1:p.Ser663=
XM_017021584.1:c.1908C>T	XP_016877073.1:p.Ser636=
XM_017021585.1:c.1857C>T	XP_016877074.1:p.Ser619=
XM_017021586.1:c.1533C>T	XP_016877075.1:p.Ser511=
XM_017021587.1:c.1533C>T	XP_016877076.1:p.Ser511=
XM_017021588.1:c.1533C>T	XP_016877077.1:p.Ser511=
NM_001164749.2:c.1839C>T MANE Select	NP_001158221.1:p.Ser613=
NM_001165893.2:c.1749C>T	NP_001159365.1:p.Ser583=
NM_022123.3:c.1743C>T	NP_071406.1:p.Ser581=
NM_173159.3:c.1800C>T	NP_775182.1:p.Ser600=
NM_001394988.1:c.1794C>T	NP_001381917.1:p.Ser598=
NM_001394989.1:c.1740C>T	NP_001381918.1:p.Ser580=