Canonical Allele Identifier: CA389412161

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269259C>G (hg19) ; chr14:g.33800053C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800053C>G , CM000676.2:g.33800053C>G	GRCh38
NC_000014.8:g.34269259C>G , CM000676.1:g.34269259C>G	GRCh37
NC_000014.7:g.33339010C>G	NCBI36
NG_013036.1:g.865801C>G
NG_013036.2:g.865801C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1746C>G MANE Select	ENSP00000348460.4:p.Asp582Glu
ENST00000551634.6:c.1755C>G	ENSP00000448373.2:p.Asp585Glu
ENST00000680362.1:c.1646C>G
ENST00000681323.1:c.793+2472C>G
ENST00000346562.6:c.1650C>G	ENSP00000319610.5:p.Asp550Glu
ENST00000356141.8:c.1746C>G	ENSP00000348460.4:p.Asp582Glu
ENST00000357798.9:c.1707C>G	ENSP00000350446.5:p.Asp569Glu
ENST00000548645.5:c.1656C>G	ENSP00000448916.1:p.Asp552Glu
ENST00000551492.5:c.1761C>G	ENSP00000450392.1:p.Asp587Glu
ENST00000551634.5:c.1668C>G	ENSP00000448373.1:p.Asp556Glu
NM_001164749.1:c.1746C>G	NP_001158221.1:p.Asp582Glu
NM_001165893.1:c.1656C>G	NP_001159365.1:p.Asp552Glu
NM_022123.2:c.1650C>G	NP_071406.1:p.Asp550Glu
NM_173159.2:c.1707C>G	NP_775182.1:p.Asp569Glu
XM_005267991.2:c.1767C>G	XP_005268048.1:p.Asp589Glu
XM_005267992.2:c.1761C>G	XP_005268049.1:p.Asp587Glu
XM_005267993.2:c.1707C>G	XP_005268050.1:p.Asp569Glu
XM_011537067.1:c.1797C>G	XP_011535369.1:p.Asp599Glu
XM_011537068.1:c.1788C>G	XP_011535370.1:p.Asp596Glu
XM_011537069.1:c.1758C>G	XP_011535371.1:p.Asp586Glu
XM_011537070.1:c.1701C>G	XP_011535372.1:p.Asp567Glu
XM_011537071.1:c.1668C>G	XP_011535373.1:p.Asp556Glu
XM_011537072.1:c.1647C>G	XP_011535374.1:p.Asp549Glu
XM_011537073.1:c.1440C>G	XP_011535375.1:p.Asp480Glu
XM_011537074.1:c.1440C>G	XP_011535376.1:p.Asp480Glu
XM_005267991.3:c.1854C>G	XP_005268048.2:p.Asp618Glu
XM_005267992.3:c.1848C>G	XP_005268049.2:p.Asp616Glu
XM_011537067.2:c.1797C>G	XP_011535369.1:p.Asp599Glu
XM_011537069.2:c.1845C>G	XP_011535371.2:p.Asp615Glu
XM_011537070.2:c.1701C>G	XP_011535372.1:p.Asp567Glu
XM_011537071.2:c.1755C>G	XP_011535373.2:p.Asp585Glu
XM_011537072.2:c.1647C>G	XP_011535374.1:p.Asp549Glu
XM_017021582.1:c.1905C>G	XP_016877071.1:p.Asp635Glu
XM_017021583.1:c.1896C>G	XP_016877072.1:p.Asp632Glu
XM_017021584.1:c.1815C>G	XP_016877073.1:p.Asp605Glu
XM_017021585.1:c.1764C>G	XP_016877074.1:p.Asp588Glu
XM_017021586.1:c.1440C>G	XP_016877075.1:p.Asp480Glu
XM_017021587.1:c.1440C>G	XP_016877076.1:p.Asp480Glu
XM_017021588.1:c.1440C>G	XP_016877077.1:p.Asp480Glu
NM_001164749.2:c.1746C>G MANE Select	NP_001158221.1:p.Asp582Glu
NM_001165893.2:c.1656C>G	NP_001159365.1:p.Asp552Glu
NM_022123.3:c.1650C>G	NP_071406.1:p.Asp550Glu
NM_173159.3:c.1707C>G	NP_775182.1:p.Asp569Glu
NM_001394988.1:c.1701C>G	NP_001381917.1:p.Asp567Glu
NM_001394989.1:c.1647C>G	NP_001381918.1:p.Asp549Glu