Canonical Allele Identifier: CA389412173

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269261C>G (hg19) ; chr14:g.33800055C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800055C>G , CM000676.2:g.33800055C>G	GRCh38
NC_000014.8:g.34269261C>G , CM000676.1:g.34269261C>G	GRCh37
NC_000014.7:g.33339012C>G	NCBI36
NG_013036.1:g.865803C>G
NG_013036.2:g.865803C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1748C>G MANE Select	ENSP00000348460.4:p.Ser583Trp
ENST00000551634.6:c.1757C>G	ENSP00000448373.2:p.Ser586Trp
ENST00000680362.1:c.1648C>G
ENST00000681323.1:c.793+2474C>G
ENST00000346562.6:c.1652C>G	ENSP00000319610.5:p.Ser551Trp
ENST00000356141.8:c.1748C>G	ENSP00000348460.4:p.Ser583Trp
ENST00000357798.9:c.1709C>G	ENSP00000350446.5:p.Ser570Trp
ENST00000548645.5:c.1658C>G	ENSP00000448916.1:p.Ser553Trp
ENST00000551492.5:c.1763C>G	ENSP00000450392.1:p.Ser588Trp
ENST00000551634.5:c.1670C>G	ENSP00000448373.1:p.Ser557Trp
NM_001164749.1:c.1748C>G	NP_001158221.1:p.Ser583Trp
NM_001165893.1:c.1658C>G	NP_001159365.1:p.Ser553Trp
NM_022123.2:c.1652C>G	NP_071406.1:p.Ser551Trp
NM_173159.2:c.1709C>G	NP_775182.1:p.Ser570Trp
XM_005267991.2:c.1769C>G	XP_005268048.1:p.Ser590Trp
XM_005267992.2:c.1763C>G	XP_005268049.1:p.Ser588Trp
XM_005267993.2:c.1709C>G	XP_005268050.1:p.Ser570Trp
XM_011537067.1:c.1799C>G	XP_011535369.1:p.Ser600Trp
XM_011537068.1:c.1790C>G	XP_011535370.1:p.Ser597Trp
XM_011537069.1:c.1760C>G	XP_011535371.1:p.Ser587Trp
XM_011537070.1:c.1703C>G	XP_011535372.1:p.Ser568Trp
XM_011537071.1:c.1670C>G	XP_011535373.1:p.Ser557Trp
XM_011537072.1:c.1649C>G	XP_011535374.1:p.Ser550Trp
XM_011537073.1:c.1442C>G	XP_011535375.1:p.Ser481Trp
XM_011537074.1:c.1442C>G	XP_011535376.1:p.Ser481Trp
XM_005267991.3:c.1856C>G	XP_005268048.2:p.Ser619Trp
XM_005267992.3:c.1850C>G	XP_005268049.2:p.Ser617Trp
XM_011537067.2:c.1799C>G	XP_011535369.1:p.Ser600Trp
XM_011537069.2:c.1847C>G	XP_011535371.2:p.Ser616Trp
XM_011537070.2:c.1703C>G	XP_011535372.1:p.Ser568Trp
XM_011537071.2:c.1757C>G	XP_011535373.2:p.Ser586Trp
XM_011537072.2:c.1649C>G	XP_011535374.1:p.Ser550Trp
XM_017021582.1:c.1907C>G	XP_016877071.1:p.Ser636Trp
XM_017021583.1:c.1898C>G	XP_016877072.1:p.Ser633Trp
XM_017021584.1:c.1817C>G	XP_016877073.1:p.Ser606Trp
XM_017021585.1:c.1766C>G	XP_016877074.1:p.Ser589Trp
XM_017021586.1:c.1442C>G	XP_016877075.1:p.Ser481Trp
XM_017021587.1:c.1442C>G	XP_016877076.1:p.Ser481Trp
XM_017021588.1:c.1442C>G	XP_016877077.1:p.Ser481Trp
NM_001164749.2:c.1748C>G MANE Select	NP_001158221.1:p.Ser583Trp
NM_001165893.2:c.1658C>G	NP_001159365.1:p.Ser553Trp
NM_022123.3:c.1652C>G	NP_071406.1:p.Ser551Trp
NM_173159.3:c.1709C>G	NP_775182.1:p.Ser570Trp
NM_001394988.1:c.1703C>G	NP_001381917.1:p.Ser568Trp
NM_001394989.1:c.1649C>G	NP_001381918.1:p.Ser550Trp