Canonical Allele Identifier: CA389412695

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269344A>G (hg19) ; chr14:g.33800138A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800138A>G , CM000676.2:g.33800138A>G	GRCh38
NC_000014.8:g.34269344A>G , CM000676.1:g.34269344A>G	GRCh37
NC_000014.7:g.33339095A>G	NCBI36
NG_013036.1:g.865886A>G
NG_013036.2:g.865886A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1831A>G MANE Select	ENSP00000348460.4:p.Ser611Gly
ENST00000551634.6:c.1840A>G	ENSP00000448373.2:p.Ser614Gly
ENST00000680362.1:c.1731A>G
ENST00000681323.1:c.793+2557A>G
ENST00000346562.6:c.1735A>G	ENSP00000319610.5:p.Ser579Gly
ENST00000356141.8:c.1831A>G	ENSP00000348460.4:p.Ser611Gly
ENST00000357798.9:c.1792A>G	ENSP00000350446.5:p.Ser598Gly
ENST00000548645.5:c.1741A>G	ENSP00000448916.1:p.Ser581Gly
ENST00000551492.5:c.1846A>G	ENSP00000450392.1:p.Ser616Gly
ENST00000551634.5:c.1753A>G	ENSP00000448373.1:p.Ser585Gly
NM_001164749.1:c.1831A>G	NP_001158221.1:p.Ser611Gly
NM_001165893.1:c.1741A>G	NP_001159365.1:p.Ser581Gly
NM_022123.2:c.1735A>G	NP_071406.1:p.Ser579Gly
NM_173159.2:c.1792A>G	NP_775182.1:p.Ser598Gly
XM_005267991.2:c.1852A>G	XP_005268048.1:p.Ser618Gly
XM_005267992.2:c.1846A>G	XP_005268049.1:p.Ser616Gly
XM_005267993.2:c.1792A>G	XP_005268050.1:p.Ser598Gly
XM_011537067.1:c.1882A>G	XP_011535369.1:p.Ser628Gly
XM_011537068.1:c.1873A>G	XP_011535370.1:p.Ser625Gly
XM_011537069.1:c.1843A>G	XP_011535371.1:p.Ser615Gly
XM_011537070.1:c.1786A>G	XP_011535372.1:p.Ser596Gly
XM_011537071.1:c.1753A>G	XP_011535373.1:p.Ser585Gly
XM_011537072.1:c.1732A>G	XP_011535374.1:p.Ser578Gly
XM_011537073.1:c.1525A>G	XP_011535375.1:p.Ser509Gly
XM_011537074.1:c.1525A>G	XP_011535376.1:p.Ser509Gly
XM_005267991.3:c.1939A>G	XP_005268048.2:p.Ser647Gly
XM_005267992.3:c.1933A>G	XP_005268049.2:p.Ser645Gly
XM_011537067.2:c.1882A>G	XP_011535369.1:p.Ser628Gly
XM_011537069.2:c.1930A>G	XP_011535371.2:p.Ser644Gly
XM_011537070.2:c.1786A>G	XP_011535372.1:p.Ser596Gly
XM_011537071.2:c.1840A>G	XP_011535373.2:p.Ser614Gly
XM_011537072.2:c.1732A>G	XP_011535374.1:p.Ser578Gly
XM_017021582.1:c.1990A>G	XP_016877071.1:p.Ser664Gly
XM_017021583.1:c.1981A>G	XP_016877072.1:p.Ser661Gly
XM_017021584.1:c.1900A>G	XP_016877073.1:p.Ser634Gly
XM_017021585.1:c.1849A>G	XP_016877074.1:p.Ser617Gly
XM_017021586.1:c.1525A>G	XP_016877075.1:p.Ser509Gly
XM_017021587.1:c.1525A>G	XP_016877076.1:p.Ser509Gly
XM_017021588.1:c.1525A>G	XP_016877077.1:p.Ser509Gly
NM_001164749.2:c.1831A>G MANE Select	NP_001158221.1:p.Ser611Gly
NM_001165893.2:c.1741A>G	NP_001159365.1:p.Ser581Gly
NM_022123.3:c.1735A>G	NP_071406.1:p.Ser579Gly
NM_173159.3:c.1792A>G	NP_775182.1:p.Ser598Gly
NM_001394988.1:c.1786A>G	NP_001381917.1:p.Ser596Gly
NM_001394989.1:c.1732A>G	NP_001381918.1:p.Ser578Gly