Canonical Allele Identifier: CA389412708

Gene: NPAS3

Linked Data

• gnomAD v4: 14-33800140-C-A
• MyVariant Identifiers: chr14:g.34269346C>A (hg19) ; chr14:g.33800140C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800140C>A , CM000676.2:g.33800140C>A	GRCh38
NC_000014.8:g.34269346C>A , CM000676.1:g.34269346C>A	GRCh37
NC_000014.7:g.33339097C>A	NCBI36
NG_013036.1:g.865888C>A
NG_013036.2:g.865888C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1833C>A MANE Select	ENSP00000348460.4:p.Ser611Arg
ENST00000551634.6:c.1842C>A	ENSP00000448373.2:p.Ser614Arg
ENST00000680362.1:c.1733C>A
ENST00000681323.1:c.793+2559C>A
ENST00000346562.6:c.1737C>A	ENSP00000319610.5:p.Ser579Arg
ENST00000356141.8:c.1833C>A	ENSP00000348460.4:p.Ser611Arg
ENST00000357798.9:c.1794C>A	ENSP00000350446.5:p.Ser598Arg
ENST00000548645.5:c.1743C>A	ENSP00000448916.1:p.Ser581Arg
ENST00000551492.5:c.1848C>A	ENSP00000450392.1:p.Ser616Arg
ENST00000551634.5:c.1755C>A	ENSP00000448373.1:p.Ser585Arg
NM_001164749.1:c.1833C>A	NP_001158221.1:p.Ser611Arg
NM_001165893.1:c.1743C>A	NP_001159365.1:p.Ser581Arg
NM_022123.2:c.1737C>A	NP_071406.1:p.Ser579Arg
NM_173159.2:c.1794C>A	NP_775182.1:p.Ser598Arg
XM_005267991.2:c.1854C>A	XP_005268048.1:p.Ser618Arg
XM_005267992.2:c.1848C>A	XP_005268049.1:p.Ser616Arg
XM_005267993.2:c.1794C>A	XP_005268050.1:p.Ser598Arg
XM_011537067.1:c.1884C>A	XP_011535369.1:p.Ser628Arg
XM_011537068.1:c.1875C>A	XP_011535370.1:p.Ser625Arg
XM_011537069.1:c.1845C>A	XP_011535371.1:p.Ser615Arg
XM_011537070.1:c.1788C>A	XP_011535372.1:p.Ser596Arg
XM_011537071.1:c.1755C>A	XP_011535373.1:p.Ser585Arg
XM_011537072.1:c.1734C>A	XP_011535374.1:p.Ser578Arg
XM_011537073.1:c.1527C>A	XP_011535375.1:p.Ser509Arg
XM_011537074.1:c.1527C>A	XP_011535376.1:p.Ser509Arg
XM_005267991.3:c.1941C>A	XP_005268048.2:p.Ser647Arg
XM_005267992.3:c.1935C>A	XP_005268049.2:p.Ser645Arg
XM_011537067.2:c.1884C>A	XP_011535369.1:p.Ser628Arg
XM_011537069.2:c.1932C>A	XP_011535371.2:p.Ser644Arg
XM_011537070.2:c.1788C>A	XP_011535372.1:p.Ser596Arg
XM_011537071.2:c.1842C>A	XP_011535373.2:p.Ser614Arg
XM_011537072.2:c.1734C>A	XP_011535374.1:p.Ser578Arg
XM_017021582.1:c.1992C>A	XP_016877071.1:p.Ser664Arg
XM_017021583.1:c.1983C>A	XP_016877072.1:p.Ser661Arg
XM_017021584.1:c.1902C>A	XP_016877073.1:p.Ser634Arg
XM_017021585.1:c.1851C>A	XP_016877074.1:p.Ser617Arg
XM_017021586.1:c.1527C>A	XP_016877075.1:p.Ser509Arg
XM_017021587.1:c.1527C>A	XP_016877076.1:p.Ser509Arg
XM_017021588.1:c.1527C>A	XP_016877077.1:p.Ser509Arg
NM_001164749.2:c.1833C>A MANE Select	NP_001158221.1:p.Ser611Arg
NM_001165893.2:c.1743C>A	NP_001159365.1:p.Ser581Arg
NM_022123.3:c.1737C>A	NP_071406.1:p.Ser579Arg
NM_173159.3:c.1794C>A	NP_775182.1:p.Ser598Arg
NM_001394988.1:c.1788C>A	NP_001381917.1:p.Ser596Arg
NM_001394989.1:c.1734C>A	NP_001381918.1:p.Ser578Arg