Canonical Allele Identifier: CA389412830

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269366C>A (hg19) ; chr14:g.33800160C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800160C>A , CM000676.2:g.33800160C>A	GRCh38
NC_000014.8:g.34269366C>A , CM000676.1:g.34269366C>A	GRCh37
NC_000014.7:g.33339117C>A	NCBI36
NG_013036.1:g.865908C>A
NG_013036.2:g.865908C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1853C>A MANE Select	ENSP00000348460.4:p.Ser618Tyr
ENST00000551634.6:c.1862C>A	ENSP00000448373.2:p.Ser621Tyr
ENST00000680362.1:c.1753C>A
ENST00000681323.1:c.793+2579C>A
ENST00000346562.6:c.1757C>A	ENSP00000319610.5:p.Ser586Tyr
ENST00000356141.8:c.1853C>A	ENSP00000348460.4:p.Ser618Tyr
ENST00000357798.9:c.1814C>A	ENSP00000350446.5:p.Ser605Tyr
ENST00000548645.5:c.1763C>A	ENSP00000448916.1:p.Ser588Tyr
ENST00000551492.5:c.1868C>A	ENSP00000450392.1:p.Ser623Tyr
ENST00000551634.5:c.1775C>A	ENSP00000448373.1:p.Ser592Tyr
NM_001164749.1:c.1853C>A	NP_001158221.1:p.Ser618Tyr
NM_001165893.1:c.1763C>A	NP_001159365.1:p.Ser588Tyr
NM_022123.2:c.1757C>A	NP_071406.1:p.Ser586Tyr
NM_173159.2:c.1814C>A	NP_775182.1:p.Ser605Tyr
XM_005267991.2:c.1874C>A	XP_005268048.1:p.Ser625Tyr
XM_005267992.2:c.1868C>A	XP_005268049.1:p.Ser623Tyr
XM_005267993.2:c.1814C>A	XP_005268050.1:p.Ser605Tyr
XM_011537067.1:c.1904C>A	XP_011535369.1:p.Ser635Tyr
XM_011537068.1:c.1895C>A	XP_011535370.1:p.Ser632Tyr
XM_011537069.1:c.1865C>A	XP_011535371.1:p.Ser622Tyr
XM_011537070.1:c.1808C>A	XP_011535372.1:p.Ser603Tyr
XM_011537071.1:c.1775C>A	XP_011535373.1:p.Ser592Tyr
XM_011537072.1:c.1754C>A	XP_011535374.1:p.Ser585Tyr
XM_011537073.1:c.1547C>A	XP_011535375.1:p.Ser516Tyr
XM_011537074.1:c.1547C>A	XP_011535376.1:p.Ser516Tyr
XM_005267991.3:c.1961C>A	XP_005268048.2:p.Ser654Tyr
XM_005267992.3:c.1955C>A	XP_005268049.2:p.Ser652Tyr
XM_011537067.2:c.1904C>A	XP_011535369.1:p.Ser635Tyr
XM_011537069.2:c.1952C>A	XP_011535371.2:p.Ser651Tyr
XM_011537070.2:c.1808C>A	XP_011535372.1:p.Ser603Tyr
XM_011537071.2:c.1862C>A	XP_011535373.2:p.Ser621Tyr
XM_011537072.2:c.1754C>A	XP_011535374.1:p.Ser585Tyr
XM_017021582.1:c.2012C>A	XP_016877071.1:p.Ser671Tyr
XM_017021583.1:c.2003C>A	XP_016877072.1:p.Ser668Tyr
XM_017021584.1:c.1922C>A	XP_016877073.1:p.Ser641Tyr
XM_017021585.1:c.1871C>A	XP_016877074.1:p.Ser624Tyr
XM_017021586.1:c.1547C>A	XP_016877075.1:p.Ser516Tyr
XM_017021587.1:c.1547C>A	XP_016877076.1:p.Ser516Tyr
XM_017021588.1:c.1547C>A	XP_016877077.1:p.Ser516Tyr
NM_001164749.2:c.1853C>A MANE Select	NP_001158221.1:p.Ser618Tyr
NM_001165893.2:c.1763C>A	NP_001159365.1:p.Ser588Tyr
NM_022123.3:c.1757C>A	NP_071406.1:p.Ser586Tyr
NM_173159.3:c.1814C>A	NP_775182.1:p.Ser605Tyr
NM_001394988.1:c.1808C>A	NP_001381917.1:p.Ser603Tyr
NM_001394989.1:c.1754C>A	NP_001381918.1:p.Ser585Tyr