Canonical Allele Identifier: CA389413234

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269465A>C (hg19) ; chr14:g.33800259A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800259A>C , CM000676.2:g.33800259A>C	GRCh38
NC_000014.8:g.34269465A>C , CM000676.1:g.34269465A>C	GRCh37
NC_000014.7:g.33339216A>C	NCBI36
NG_013036.1:g.866007A>C
NG_013036.2:g.866007A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1952A>C MANE Select	ENSP00000348460.4:p.Glu651Ala
ENST00000551634.6:c.1961A>C	ENSP00000448373.2:p.Glu654Ala
ENST00000680362.1:c.1852A>C
ENST00000681323.1:c.793+2678A>C
ENST00000346562.6:c.1856A>C	ENSP00000319610.5:p.Glu619Ala
ENST00000356141.8:c.1952A>C	ENSP00000348460.4:p.Glu651Ala
ENST00000357798.9:c.1913A>C	ENSP00000350446.5:p.Glu638Ala
ENST00000548645.5:c.1862A>C	ENSP00000448916.1:p.Glu621Ala
ENST00000551492.5:c.1967A>C	ENSP00000450392.1:p.Glu656Ala
ENST00000551634.5:c.1874A>C	ENSP00000448373.1:p.Glu625Ala
NM_001164749.1:c.1952A>C	NP_001158221.1:p.Glu651Ala
NM_001165893.1:c.1862A>C	NP_001159365.1:p.Glu621Ala
NM_022123.2:c.1856A>C	NP_071406.1:p.Glu619Ala
NM_173159.2:c.1913A>C	NP_775182.1:p.Glu638Ala
XM_005267991.2:c.1973A>C	XP_005268048.1:p.Glu658Ala
XM_005267992.2:c.1967A>C	XP_005268049.1:p.Glu656Ala
XM_005267993.2:c.1913A>C	XP_005268050.1:p.Glu638Ala
XM_011537067.1:c.2003A>C	XP_011535369.1:p.Glu668Ala
XM_011537068.1:c.1994A>C	XP_011535370.1:p.Glu665Ala
XM_011537069.1:c.1964A>C	XP_011535371.1:p.Glu655Ala
XM_011537070.1:c.1907A>C	XP_011535372.1:p.Glu636Ala
XM_011537071.1:c.1874A>C	XP_011535373.1:p.Glu625Ala
XM_011537072.1:c.1853A>C	XP_011535374.1:p.Glu618Ala
XM_011537073.1:c.1646A>C	XP_011535375.1:p.Glu549Ala
XM_011537074.1:c.1646A>C	XP_011535376.1:p.Glu549Ala
XM_005267991.3:c.2060A>C	XP_005268048.2:p.Glu687Ala
XM_005267992.3:c.2054A>C	XP_005268049.2:p.Glu685Ala
XM_011537067.2:c.2003A>C	XP_011535369.1:p.Glu668Ala
XM_011537069.2:c.2051A>C	XP_011535371.2:p.Glu684Ala
XM_011537070.2:c.1907A>C	XP_011535372.1:p.Glu636Ala
XM_011537071.2:c.1961A>C	XP_011535373.2:p.Glu654Ala
XM_011537072.2:c.1853A>C	XP_011535374.1:p.Glu618Ala
XM_017021582.1:c.2111A>C	XP_016877071.1:p.Glu704Ala
XM_017021583.1:c.2102A>C	XP_016877072.1:p.Glu701Ala
XM_017021584.1:c.2021A>C	XP_016877073.1:p.Glu674Ala
XM_017021585.1:c.1970A>C	XP_016877074.1:p.Glu657Ala
XM_017021586.1:c.1646A>C	XP_016877075.1:p.Glu549Ala
XM_017021587.1:c.1646A>C	XP_016877076.1:p.Glu549Ala
XM_017021588.1:c.1646A>C	XP_016877077.1:p.Glu549Ala
NM_001164749.2:c.1952A>C MANE Select	NP_001158221.1:p.Glu651Ala
NM_001165893.2:c.1862A>C	NP_001159365.1:p.Glu621Ala
NM_022123.3:c.1856A>C	NP_071406.1:p.Glu619Ala
NM_173159.3:c.1913A>C	NP_775182.1:p.Glu638Ala
NM_001394988.1:c.1907A>C	NP_001381917.1:p.Glu636Ala
NM_001394989.1:c.1853A>C	NP_001381918.1:p.Glu618Ala