Canonical Allele Identifier: CA389412167

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269260T>G (hg19) ; chr14:g.33800054T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800054T>G , CM000676.2:g.33800054T>G	GRCh38
NC_000014.8:g.34269260T>G , CM000676.1:g.34269260T>G	GRCh37
NC_000014.7:g.33339011T>G	NCBI36
NG_013036.1:g.865802T>G
NG_013036.2:g.865802T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1747T>G MANE Select	ENSP00000348460.4:p.Ser583Ala
ENST00000551634.6:c.1756T>G	ENSP00000448373.2:p.Ser586Ala
ENST00000680362.1:c.1647T>G
ENST00000681323.1:c.793+2473T>G
ENST00000346562.6:c.1651T>G	ENSP00000319610.5:p.Ser551Ala
ENST00000356141.8:c.1747T>G	ENSP00000348460.4:p.Ser583Ala
ENST00000357798.9:c.1708T>G	ENSP00000350446.5:p.Ser570Ala
ENST00000548645.5:c.1657T>G	ENSP00000448916.1:p.Ser553Ala
ENST00000551492.5:c.1762T>G	ENSP00000450392.1:p.Ser588Ala
ENST00000551634.5:c.1669T>G	ENSP00000448373.1:p.Ser557Ala
NM_001164749.1:c.1747T>G	NP_001158221.1:p.Ser583Ala
NM_001165893.1:c.1657T>G	NP_001159365.1:p.Ser553Ala
NM_022123.2:c.1651T>G	NP_071406.1:p.Ser551Ala
NM_173159.2:c.1708T>G	NP_775182.1:p.Ser570Ala
XM_005267991.2:c.1768T>G	XP_005268048.1:p.Ser590Ala
XM_005267992.2:c.1762T>G	XP_005268049.1:p.Ser588Ala
XM_005267993.2:c.1708T>G	XP_005268050.1:p.Ser570Ala
XM_011537067.1:c.1798T>G	XP_011535369.1:p.Ser600Ala
XM_011537068.1:c.1789T>G	XP_011535370.1:p.Ser597Ala
XM_011537069.1:c.1759T>G	XP_011535371.1:p.Ser587Ala
XM_011537070.1:c.1702T>G	XP_011535372.1:p.Ser568Ala
XM_011537071.1:c.1669T>G	XP_011535373.1:p.Ser557Ala
XM_011537072.1:c.1648T>G	XP_011535374.1:p.Ser550Ala
XM_011537073.1:c.1441T>G	XP_011535375.1:p.Ser481Ala
XM_011537074.1:c.1441T>G	XP_011535376.1:p.Ser481Ala
XM_005267991.3:c.1855T>G	XP_005268048.2:p.Ser619Ala
XM_005267992.3:c.1849T>G	XP_005268049.2:p.Ser617Ala
XM_011537067.2:c.1798T>G	XP_011535369.1:p.Ser600Ala
XM_011537069.2:c.1846T>G	XP_011535371.2:p.Ser616Ala
XM_011537070.2:c.1702T>G	XP_011535372.1:p.Ser568Ala
XM_011537071.2:c.1756T>G	XP_011535373.2:p.Ser586Ala
XM_011537072.2:c.1648T>G	XP_011535374.1:p.Ser550Ala
XM_017021582.1:c.1906T>G	XP_016877071.1:p.Ser636Ala
XM_017021583.1:c.1897T>G	XP_016877072.1:p.Ser633Ala
XM_017021584.1:c.1816T>G	XP_016877073.1:p.Ser606Ala
XM_017021585.1:c.1765T>G	XP_016877074.1:p.Ser589Ala
XM_017021586.1:c.1441T>G	XP_016877075.1:p.Ser481Ala
XM_017021587.1:c.1441T>G	XP_016877076.1:p.Ser481Ala
XM_017021588.1:c.1441T>G	XP_016877077.1:p.Ser481Ala
NM_001164749.2:c.1747T>G MANE Select	NP_001158221.1:p.Ser583Ala
NM_001165893.2:c.1657T>G	NP_001159365.1:p.Ser553Ala
NM_022123.3:c.1651T>G	NP_071406.1:p.Ser551Ala
NM_173159.3:c.1708T>G	NP_775182.1:p.Ser570Ala
NM_001394988.1:c.1702T>G	NP_001381917.1:p.Ser568Ala
NM_001394989.1:c.1648T>G	NP_001381918.1:p.Ser550Ala