Canonical Allele Identifier: CA389413549

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269534C>A (hg19) ; chr14:g.33800328C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800328C>A , CM000676.2:g.33800328C>A	GRCh38
NC_000014.8:g.34269534C>A , CM000676.1:g.34269534C>A	GRCh37
NC_000014.7:g.33339285C>A	NCBI36
NG_013036.1:g.866076C>A
NG_013036.2:g.866076C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2021C>A MANE Select	ENSP00000348460.4:p.Ser674Tyr
ENST00000551634.6:c.2030C>A	ENSP00000448373.2:p.Ser677Tyr
ENST00000680362.1:c.1921C>A
ENST00000681323.1:c.793+2747C>A
ENST00000346562.6:c.1925C>A	ENSP00000319610.5:p.Ser642Tyr
ENST00000356141.8:c.2021C>A	ENSP00000348460.4:p.Ser674Tyr
ENST00000357798.9:c.1982C>A	ENSP00000350446.5:p.Ser661Tyr
ENST00000548645.5:c.1931C>A	ENSP00000448916.1:p.Ser644Tyr
ENST00000551492.5:c.2036C>A	ENSP00000450392.1:p.Ser679Tyr
ENST00000551634.5:c.1943C>A	ENSP00000448373.1:p.Ser648Tyr
NM_001164749.1:c.2021C>A	NP_001158221.1:p.Ser674Tyr
NM_001165893.1:c.1931C>A	NP_001159365.1:p.Ser644Tyr
NM_022123.2:c.1925C>A	NP_071406.1:p.Ser642Tyr
NM_173159.2:c.1982C>A	NP_775182.1:p.Ser661Tyr
XM_005267991.2:c.2042C>A	XP_005268048.1:p.Ser681Tyr
XM_005267992.2:c.2036C>A	XP_005268049.1:p.Ser679Tyr
XM_005267993.2:c.1982C>A	XP_005268050.1:p.Ser661Tyr
XM_011537067.1:c.2072C>A	XP_011535369.1:p.Ser691Tyr
XM_011537068.1:c.2063C>A	XP_011535370.1:p.Ser688Tyr
XM_011537069.1:c.2033C>A	XP_011535371.1:p.Ser678Tyr
XM_011537070.1:c.1976C>A	XP_011535372.1:p.Ser659Tyr
XM_011537071.1:c.1943C>A	XP_011535373.1:p.Ser648Tyr
XM_011537072.1:c.1922C>A	XP_011535374.1:p.Ser641Tyr
XM_011537073.1:c.1715C>A	XP_011535375.1:p.Ser572Tyr
XM_011537074.1:c.1715C>A	XP_011535376.1:p.Ser572Tyr
XM_005267991.3:c.2129C>A	XP_005268048.2:p.Ser710Tyr
XM_005267992.3:c.2123C>A	XP_005268049.2:p.Ser708Tyr
XM_011537067.2:c.2072C>A	XP_011535369.1:p.Ser691Tyr
XM_011537069.2:c.2120C>A	XP_011535371.2:p.Ser707Tyr
XM_011537070.2:c.1976C>A	XP_011535372.1:p.Ser659Tyr
XM_011537071.2:c.2030C>A	XP_011535373.2:p.Ser677Tyr
XM_011537072.2:c.1922C>A	XP_011535374.1:p.Ser641Tyr
XM_017021582.1:c.2180C>A	XP_016877071.1:p.Ser727Tyr
XM_017021583.1:c.2171C>A	XP_016877072.1:p.Ser724Tyr
XM_017021584.1:c.2090C>A	XP_016877073.1:p.Ser697Tyr
XM_017021585.1:c.2039C>A	XP_016877074.1:p.Ser680Tyr
XM_017021586.1:c.1715C>A	XP_016877075.1:p.Ser572Tyr
XM_017021587.1:c.1715C>A	XP_016877076.1:p.Ser572Tyr
XM_017021588.1:c.1715C>A	XP_016877077.1:p.Ser572Tyr
NM_001164749.2:c.2021C>A MANE Select	NP_001158221.1:p.Ser674Tyr
NM_001165893.2:c.1931C>A	NP_001159365.1:p.Ser644Tyr
NM_022123.3:c.1925C>A	NP_071406.1:p.Ser642Tyr
NM_173159.3:c.1982C>A	NP_775182.1:p.Ser661Tyr
NM_001394988.1:c.1976C>A	NP_001381917.1:p.Ser659Tyr
NM_001394989.1:c.1922C>A	NP_001381918.1:p.Ser641Tyr