Canonical Allele Identifier: CA389412855

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269372C>A (hg19) ; chr14:g.33800166C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800166C>A , CM000676.2:g.33800166C>A	GRCh38
NC_000014.8:g.34269372C>A , CM000676.1:g.34269372C>A	GRCh37
NC_000014.7:g.33339123C>A	NCBI36
NG_013036.1:g.865914C>A
NG_013036.2:g.865914C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1859C>A MANE Select	ENSP00000348460.4:p.Ala620Glu
ENST00000551634.6:c.1868C>A	ENSP00000448373.2:p.Ala623Glu
ENST00000680362.1:c.1759C>A
ENST00000681323.1:c.793+2585C>A
ENST00000346562.6:c.1763C>A	ENSP00000319610.5:p.Ala588Glu
ENST00000356141.8:c.1859C>A	ENSP00000348460.4:p.Ala620Glu
ENST00000357798.9:c.1820C>A	ENSP00000350446.5:p.Ala607Glu
ENST00000548645.5:c.1769C>A	ENSP00000448916.1:p.Ala590Glu
ENST00000551492.5:c.1874C>A	ENSP00000450392.1:p.Ala625Glu
ENST00000551634.5:c.1781C>A	ENSP00000448373.1:p.Ala594Glu
NM_001164749.1:c.1859C>A	NP_001158221.1:p.Ala620Glu
NM_001165893.1:c.1769C>A	NP_001159365.1:p.Ala590Glu
NM_022123.2:c.1763C>A	NP_071406.1:p.Ala588Glu
NM_173159.2:c.1820C>A	NP_775182.1:p.Ala607Glu
XM_005267991.2:c.1880C>A	XP_005268048.1:p.Ala627Glu
XM_005267992.2:c.1874C>A	XP_005268049.1:p.Ala625Glu
XM_005267993.2:c.1820C>A	XP_005268050.1:p.Ala607Glu
XM_011537067.1:c.1910C>A	XP_011535369.1:p.Ala637Glu
XM_011537068.1:c.1901C>A	XP_011535370.1:p.Ala634Glu
XM_011537069.1:c.1871C>A	XP_011535371.1:p.Ala624Glu
XM_011537070.1:c.1814C>A	XP_011535372.1:p.Ala605Glu
XM_011537071.1:c.1781C>A	XP_011535373.1:p.Ala594Glu
XM_011537072.1:c.1760C>A	XP_011535374.1:p.Ala587Glu
XM_011537073.1:c.1553C>A	XP_011535375.1:p.Ala518Glu
XM_011537074.1:c.1553C>A	XP_011535376.1:p.Ala518Glu
XM_005267991.3:c.1967C>A	XP_005268048.2:p.Ala656Glu
XM_005267992.3:c.1961C>A	XP_005268049.2:p.Ala654Glu
XM_011537067.2:c.1910C>A	XP_011535369.1:p.Ala637Glu
XM_011537069.2:c.1958C>A	XP_011535371.2:p.Ala653Glu
XM_011537070.2:c.1814C>A	XP_011535372.1:p.Ala605Glu
XM_011537071.2:c.1868C>A	XP_011535373.2:p.Ala623Glu
XM_011537072.2:c.1760C>A	XP_011535374.1:p.Ala587Glu
XM_017021582.1:c.2018C>A	XP_016877071.1:p.Ala673Glu
XM_017021583.1:c.2009C>A	XP_016877072.1:p.Ala670Glu
XM_017021584.1:c.1928C>A	XP_016877073.1:p.Ala643Glu
XM_017021585.1:c.1877C>A	XP_016877074.1:p.Ala626Glu
XM_017021586.1:c.1553C>A	XP_016877075.1:p.Ala518Glu
XM_017021587.1:c.1553C>A	XP_016877076.1:p.Ala518Glu
XM_017021588.1:c.1553C>A	XP_016877077.1:p.Ala518Glu
NM_001164749.2:c.1859C>A MANE Select	NP_001158221.1:p.Ala620Glu
NM_001165893.2:c.1769C>A	NP_001159365.1:p.Ala590Glu
NM_022123.3:c.1763C>A	NP_071406.1:p.Ala588Glu
NM_173159.3:c.1820C>A	NP_775182.1:p.Ala607Glu
NM_001394988.1:c.1814C>A	NP_001381917.1:p.Ala605Glu
NM_001394989.1:c.1760C>A	NP_001381918.1:p.Ala587Glu