Canonical Allele Identifier: CA486092763

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269298C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800092C>T , CM000676.2:g.33800092C>T	GRCh38
NC_000014.8:g.34269298C>T , CM000676.1:g.34269298C>T	GRCh37
NC_000014.7:g.33339049C>T	NCBI36
NG_013036.1:g.865840C>T
NG_013036.2:g.865840C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1785C>T MANE Select	ENSP00000348460.4:p.Ser595=
ENST00000551634.6:c.1794C>T	ENSP00000448373.2:p.Ser598=
ENST00000680362.1:c.1685C>T
ENST00000681323.1:c.793+2511C>T
ENST00000346562.6:c.1689C>T	ENSP00000319610.5:p.Ser563=
ENST00000356141.8:c.1785C>T	ENSP00000348460.4:p.Ser595=
ENST00000357798.9:c.1746C>T	ENSP00000350446.5:p.Ser582=
ENST00000548645.5:c.1695C>T	ENSP00000448916.1:p.Ser565=
ENST00000551492.5:c.1800C>T	ENSP00000450392.1:p.Ser600=
ENST00000551634.5:c.1707C>T	ENSP00000448373.1:p.Ser569=
NM_001164749.1:c.1785C>T	NP_001158221.1:p.Ser595=
NM_001165893.1:c.1695C>T	NP_001159365.1:p.Ser565=
NM_022123.2:c.1689C>T	NP_071406.1:p.Ser563=
NM_173159.2:c.1746C>T	NP_775182.1:p.Ser582=
XM_005267991.2:c.1806C>T	XP_005268048.1:p.Ser602=
XM_005267992.2:c.1800C>T	XP_005268049.1:p.Ser600=
XM_005267993.2:c.1746C>T	XP_005268050.1:p.Ser582=
XM_011537067.1:c.1836C>T	XP_011535369.1:p.Ser612=
XM_011537068.1:c.1827C>T	XP_011535370.1:p.Ser609=
XM_011537069.1:c.1797C>T	XP_011535371.1:p.Ser599=
XM_011537070.1:c.1740C>T	XP_011535372.1:p.Ser580=
XM_011537071.1:c.1707C>T	XP_011535373.1:p.Ser569=
XM_011537072.1:c.1686C>T	XP_011535374.1:p.Ser562=
XM_011537073.1:c.1479C>T	XP_011535375.1:p.Ser493=
XM_011537074.1:c.1479C>T	XP_011535376.1:p.Ser493=
XM_005267991.3:c.1893C>T	XP_005268048.2:p.Ser631=
XM_005267992.3:c.1887C>T	XP_005268049.2:p.Ser629=
XM_011537067.2:c.1836C>T	XP_011535369.1:p.Ser612=
XM_011537069.2:c.1884C>T	XP_011535371.2:p.Ser628=
XM_011537070.2:c.1740C>T	XP_011535372.1:p.Ser580=
XM_011537071.2:c.1794C>T	XP_011535373.2:p.Ser598=
XM_011537072.2:c.1686C>T	XP_011535374.1:p.Ser562=
XM_017021582.1:c.1944C>T	XP_016877071.1:p.Ser648=
XM_017021583.1:c.1935C>T	XP_016877072.1:p.Ser645=
XM_017021584.1:c.1854C>T	XP_016877073.1:p.Ser618=
XM_017021585.1:c.1803C>T	XP_016877074.1:p.Ser601=
XM_017021586.1:c.1479C>T	XP_016877075.1:p.Ser493=
XM_017021587.1:c.1479C>T	XP_016877076.1:p.Ser493=
XM_017021588.1:c.1479C>T	XP_016877077.1:p.Ser493=
NM_001164749.2:c.1785C>T MANE Select	NP_001158221.1:p.Ser595=
NM_001165893.2:c.1695C>T	NP_001159365.1:p.Ser565=
NM_022123.3:c.1689C>T	NP_071406.1:p.Ser563=
NM_173159.3:c.1746C>T	NP_775182.1:p.Ser582=
NM_001394988.1:c.1740C>T	NP_001381917.1:p.Ser580=
NM_001394989.1:c.1686C>T	NP_001381918.1:p.Ser562=