Canonical Allele Identifier: CA389412258

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269277G>C (hg19) ; chr14:g.33800071G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800071G>C , CM000676.2:g.33800071G>C	GRCh38
NC_000014.8:g.34269277G>C , CM000676.1:g.34269277G>C	GRCh37
NC_000014.7:g.33339028G>C	NCBI36
NG_013036.1:g.865819G>C
NG_013036.2:g.865819G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1764G>C MANE Select	ENSP00000348460.4:p.Glu588Asp
ENST00000551634.6:c.1773G>C	ENSP00000448373.2:p.Glu591Asp
ENST00000680362.1:c.1664G>C
ENST00000681323.1:c.793+2490G>C
ENST00000346562.6:c.1668G>C	ENSP00000319610.5:p.Glu556Asp
ENST00000356141.8:c.1764G>C	ENSP00000348460.4:p.Glu588Asp
ENST00000357798.9:c.1725G>C	ENSP00000350446.5:p.Glu575Asp
ENST00000548645.5:c.1674G>C	ENSP00000448916.1:p.Glu558Asp
ENST00000551492.5:c.1779G>C	ENSP00000450392.1:p.Glu593Asp
ENST00000551634.5:c.1686G>C	ENSP00000448373.1:p.Glu562Asp
NM_001164749.1:c.1764G>C	NP_001158221.1:p.Glu588Asp
NM_001165893.1:c.1674G>C	NP_001159365.1:p.Glu558Asp
NM_022123.2:c.1668G>C	NP_071406.1:p.Glu556Asp
NM_173159.2:c.1725G>C	NP_775182.1:p.Glu575Asp
XM_005267991.2:c.1785G>C	XP_005268048.1:p.Glu595Asp
XM_005267992.2:c.1779G>C	XP_005268049.1:p.Glu593Asp
XM_005267993.2:c.1725G>C	XP_005268050.1:p.Glu575Asp
XM_011537067.1:c.1815G>C	XP_011535369.1:p.Glu605Asp
XM_011537068.1:c.1806G>C	XP_011535370.1:p.Glu602Asp
XM_011537069.1:c.1776G>C	XP_011535371.1:p.Glu592Asp
XM_011537070.1:c.1719G>C	XP_011535372.1:p.Glu573Asp
XM_011537071.1:c.1686G>C	XP_011535373.1:p.Glu562Asp
XM_011537072.1:c.1665G>C	XP_011535374.1:p.Glu555Asp
XM_011537073.1:c.1458G>C	XP_011535375.1:p.Glu486Asp
XM_011537074.1:c.1458G>C	XP_011535376.1:p.Glu486Asp
XM_005267991.3:c.1872G>C	XP_005268048.2:p.Glu624Asp
XM_005267992.3:c.1866G>C	XP_005268049.2:p.Glu622Asp
XM_011537067.2:c.1815G>C	XP_011535369.1:p.Glu605Asp
XM_011537069.2:c.1863G>C	XP_011535371.2:p.Glu621Asp
XM_011537070.2:c.1719G>C	XP_011535372.1:p.Glu573Asp
XM_011537071.2:c.1773G>C	XP_011535373.2:p.Glu591Asp
XM_011537072.2:c.1665G>C	XP_011535374.1:p.Glu555Asp
XM_017021582.1:c.1923G>C	XP_016877071.1:p.Glu641Asp
XM_017021583.1:c.1914G>C	XP_016877072.1:p.Glu638Asp
XM_017021584.1:c.1833G>C	XP_016877073.1:p.Glu611Asp
XM_017021585.1:c.1782G>C	XP_016877074.1:p.Glu594Asp
XM_017021586.1:c.1458G>C	XP_016877075.1:p.Glu486Asp
XM_017021587.1:c.1458G>C	XP_016877076.1:p.Glu486Asp
XM_017021588.1:c.1458G>C	XP_016877077.1:p.Glu486Asp
NM_001164749.2:c.1764G>C MANE Select	NP_001158221.1:p.Glu588Asp
NM_001165893.2:c.1674G>C	NP_001159365.1:p.Glu558Asp
NM_022123.3:c.1668G>C	NP_071406.1:p.Glu556Asp
NM_173159.3:c.1725G>C	NP_775182.1:p.Glu575Asp
NM_001394988.1:c.1719G>C	NP_001381917.1:p.Glu573Asp
NM_001394989.1:c.1665G>C	NP_001381918.1:p.Glu555Asp