Canonical Allele Identifier: CA486093004

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269499C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800293C>T , CM000676.2:g.33800293C>T	GRCh38
NC_000014.8:g.34269499C>T , CM000676.1:g.34269499C>T	GRCh37
NC_000014.7:g.33339250C>T	NCBI36
NG_013036.1:g.866041C>T
NG_013036.2:g.866041C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1986C>T MANE Select	ENSP00000348460.4:p.Ser662=
ENST00000551634.6:c.1995C>T	ENSP00000448373.2:p.Ser665=
ENST00000680362.1:c.1886C>T
ENST00000681323.1:c.793+2712C>T
ENST00000346562.6:c.1890C>T	ENSP00000319610.5:p.Ser630=
ENST00000356141.8:c.1986C>T	ENSP00000348460.4:p.Ser662=
ENST00000357798.9:c.1947C>T	ENSP00000350446.5:p.Ser649=
ENST00000548645.5:c.1896C>T	ENSP00000448916.1:p.Ser632=
ENST00000551492.5:c.2001C>T	ENSP00000450392.1:p.Ser667=
ENST00000551634.5:c.1908C>T	ENSP00000448373.1:p.Ser636=
NM_001164749.1:c.1986C>T	NP_001158221.1:p.Ser662=
NM_001165893.1:c.1896C>T	NP_001159365.1:p.Ser632=
NM_022123.2:c.1890C>T	NP_071406.1:p.Ser630=
NM_173159.2:c.1947C>T	NP_775182.1:p.Ser649=
XM_005267991.2:c.2007C>T	XP_005268048.1:p.Ser669=
XM_005267992.2:c.2001C>T	XP_005268049.1:p.Ser667=
XM_005267993.2:c.1947C>T	XP_005268050.1:p.Ser649=
XM_011537067.1:c.2037C>T	XP_011535369.1:p.Ser679=
XM_011537068.1:c.2028C>T	XP_011535370.1:p.Ser676=
XM_011537069.1:c.1998C>T	XP_011535371.1:p.Ser666=
XM_011537070.1:c.1941C>T	XP_011535372.1:p.Ser647=
XM_011537071.1:c.1908C>T	XP_011535373.1:p.Ser636=
XM_011537072.1:c.1887C>T	XP_011535374.1:p.Ser629=
XM_011537073.1:c.1680C>T	XP_011535375.1:p.Ser560=
XM_011537074.1:c.1680C>T	XP_011535376.1:p.Ser560=
XM_005267991.3:c.2094C>T	XP_005268048.2:p.Ser698=
XM_005267992.3:c.2088C>T	XP_005268049.2:p.Ser696=
XM_011537067.2:c.2037C>T	XP_011535369.1:p.Ser679=
XM_011537069.2:c.2085C>T	XP_011535371.2:p.Ser695=
XM_011537070.2:c.1941C>T	XP_011535372.1:p.Ser647=
XM_011537071.2:c.1995C>T	XP_011535373.2:p.Ser665=
XM_011537072.2:c.1887C>T	XP_011535374.1:p.Ser629=
XM_017021582.1:c.2145C>T	XP_016877071.1:p.Ser715=
XM_017021583.1:c.2136C>T	XP_016877072.1:p.Ser712=
XM_017021584.1:c.2055C>T	XP_016877073.1:p.Ser685=
XM_017021585.1:c.2004C>T	XP_016877074.1:p.Ser668=
XM_017021586.1:c.1680C>T	XP_016877075.1:p.Ser560=
XM_017021587.1:c.1680C>T	XP_016877076.1:p.Ser560=
XM_017021588.1:c.1680C>T	XP_016877077.1:p.Ser560=
NM_001164749.2:c.1986C>T MANE Select	NP_001158221.1:p.Ser662=
NM_001165893.2:c.1896C>T	NP_001159365.1:p.Ser632=
NM_022123.3:c.1890C>T	NP_071406.1:p.Ser630=
NM_173159.3:c.1947C>T	NP_775182.1:p.Ser649=
NM_001394988.1:c.1941C>T	NP_001381917.1:p.Ser647=
NM_001394989.1:c.1887C>T	NP_001381918.1:p.Ser629=