Canonical Allele Identifier: CA389413401

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269499C>G (hg19) ; chr14:g.33800293C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1986C>G MANE Select	ENSP00000348460.4:p.Ser662Arg
ENST00000551634.6:c.1995C>G	ENSP00000448373.2:p.Ser665Arg
ENST00000680362.1:c.1886C>G
ENST00000681323.1:c.793+2712C>G
ENST00000346562.6:c.1890C>G	ENSP00000319610.5:p.Ser630Arg
ENST00000356141.8:c.1986C>G	ENSP00000348460.4:p.Ser662Arg
ENST00000357798.9:c.1947C>G	ENSP00000350446.5:p.Ser649Arg
ENST00000548645.5:c.1896C>G	ENSP00000448916.1:p.Ser632Arg
ENST00000551492.5:c.2001C>G	ENSP00000450392.1:p.Ser667Arg
ENST00000551634.5:c.1908C>G	ENSP00000448373.1:p.Ser636Arg
NM_001164749.1:c.1986C>G	NP_001158221.1:p.Ser662Arg
NM_001165893.1:c.1896C>G	NP_001159365.1:p.Ser632Arg
NM_022123.2:c.1890C>G	NP_071406.1:p.Ser630Arg
NM_173159.2:c.1947C>G	NP_775182.1:p.Ser649Arg
XM_005267991.2:c.2007C>G	XP_005268048.1:p.Ser669Arg
XM_005267992.2:c.2001C>G	XP_005268049.1:p.Ser667Arg
XM_005267993.2:c.1947C>G	XP_005268050.1:p.Ser649Arg
XM_011537067.1:c.2037C>G	XP_011535369.1:p.Ser679Arg
XM_011537068.1:c.2028C>G	XP_011535370.1:p.Ser676Arg
XM_011537069.1:c.1998C>G	XP_011535371.1:p.Ser666Arg
XM_011537070.1:c.1941C>G	XP_011535372.1:p.Ser647Arg
XM_011537071.1:c.1908C>G	XP_011535373.1:p.Ser636Arg
XM_011537072.1:c.1887C>G	XP_011535374.1:p.Ser629Arg
XM_011537073.1:c.1680C>G	XP_011535375.1:p.Ser560Arg
XM_011537074.1:c.1680C>G	XP_011535376.1:p.Ser560Arg
XM_005267991.3:c.2094C>G	XP_005268048.2:p.Ser698Arg
XM_005267992.3:c.2088C>G	XP_005268049.2:p.Ser696Arg
XM_011537067.2:c.2037C>G	XP_011535369.1:p.Ser679Arg
XM_011537069.2:c.2085C>G	XP_011535371.2:p.Ser695Arg
XM_011537070.2:c.1941C>G	XP_011535372.1:p.Ser647Arg
XM_011537071.2:c.1995C>G	XP_011535373.2:p.Ser665Arg
XM_011537072.2:c.1887C>G	XP_011535374.1:p.Ser629Arg
XM_017021582.1:c.2145C>G	XP_016877071.1:p.Ser715Arg
XM_017021583.1:c.2136C>G	XP_016877072.1:p.Ser712Arg
XM_017021584.1:c.2055C>G	XP_016877073.1:p.Ser685Arg
XM_017021585.1:c.2004C>G	XP_016877074.1:p.Ser668Arg
XM_017021586.1:c.1680C>G	XP_016877075.1:p.Ser560Arg
XM_017021587.1:c.1680C>G	XP_016877076.1:p.Ser560Arg
XM_017021588.1:c.1680C>G	XP_016877077.1:p.Ser560Arg
NM_001164749.2:c.1986C>G MANE Select	NP_001158221.1:p.Ser662Arg
NM_001165893.2:c.1896C>G	NP_001159365.1:p.Ser632Arg
NM_022123.3:c.1890C>G	NP_071406.1:p.Ser630Arg
NM_173159.3:c.1947C>G	NP_775182.1:p.Ser649Arg
NM_001394988.1:c.1941C>G	NP_001381917.1:p.Ser647Arg
NM_001394989.1:c.1887C>G	NP_001381918.1:p.Ser629Arg