Canonical Allele Identifier: CA389413351

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269490C>A (hg19) ; chr14:g.33800284C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800284C>A , CM000676.2:g.33800284C>A	GRCh38
NC_000014.8:g.34269490C>A , CM000676.1:g.34269490C>A	GRCh37
NC_000014.7:g.33339241C>A	NCBI36
NG_013036.1:g.866032C>A
NG_013036.2:g.866032C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1977C>A MANE Select	ENSP00000348460.4:p.Asp659Glu
ENST00000551634.6:c.1986C>A	ENSP00000448373.2:p.Asp662Glu
ENST00000680362.1:c.1877C>A
ENST00000681323.1:c.793+2703C>A
ENST00000346562.6:c.1881C>A	ENSP00000319610.5:p.Asp627Glu
ENST00000356141.8:c.1977C>A	ENSP00000348460.4:p.Asp659Glu
ENST00000357798.9:c.1938C>A	ENSP00000350446.5:p.Asp646Glu
ENST00000548645.5:c.1887C>A	ENSP00000448916.1:p.Asp629Glu
ENST00000551492.5:c.1992C>A	ENSP00000450392.1:p.Asp664Glu
ENST00000551634.5:c.1899C>A	ENSP00000448373.1:p.Asp633Glu
NM_001164749.1:c.1977C>A	NP_001158221.1:p.Asp659Glu
NM_001165893.1:c.1887C>A	NP_001159365.1:p.Asp629Glu
NM_022123.2:c.1881C>A	NP_071406.1:p.Asp627Glu
NM_173159.2:c.1938C>A	NP_775182.1:p.Asp646Glu
XM_005267991.2:c.1998C>A	XP_005268048.1:p.Asp666Glu
XM_005267992.2:c.1992C>A	XP_005268049.1:p.Asp664Glu
XM_005267993.2:c.1938C>A	XP_005268050.1:p.Asp646Glu
XM_011537067.1:c.2028C>A	XP_011535369.1:p.Asp676Glu
XM_011537068.1:c.2019C>A	XP_011535370.1:p.Asp673Glu
XM_011537069.1:c.1989C>A	XP_011535371.1:p.Asp663Glu
XM_011537070.1:c.1932C>A	XP_011535372.1:p.Asp644Glu
XM_011537071.1:c.1899C>A	XP_011535373.1:p.Asp633Glu
XM_011537072.1:c.1878C>A	XP_011535374.1:p.Asp626Glu
XM_011537073.1:c.1671C>A	XP_011535375.1:p.Asp557Glu
XM_011537074.1:c.1671C>A	XP_011535376.1:p.Asp557Glu
XM_005267991.3:c.2085C>A	XP_005268048.2:p.Asp695Glu
XM_005267992.3:c.2079C>A	XP_005268049.2:p.Asp693Glu
XM_011537067.2:c.2028C>A	XP_011535369.1:p.Asp676Glu
XM_011537069.2:c.2076C>A	XP_011535371.2:p.Asp692Glu
XM_011537070.2:c.1932C>A	XP_011535372.1:p.Asp644Glu
XM_011537071.2:c.1986C>A	XP_011535373.2:p.Asp662Glu
XM_011537072.2:c.1878C>A	XP_011535374.1:p.Asp626Glu
XM_017021582.1:c.2136C>A	XP_016877071.1:p.Asp712Glu
XM_017021583.1:c.2127C>A	XP_016877072.1:p.Asp709Glu
XM_017021584.1:c.2046C>A	XP_016877073.1:p.Asp682Glu
XM_017021585.1:c.1995C>A	XP_016877074.1:p.Asp665Glu
XM_017021586.1:c.1671C>A	XP_016877075.1:p.Asp557Glu
XM_017021587.1:c.1671C>A	XP_016877076.1:p.Asp557Glu
XM_017021588.1:c.1671C>A	XP_016877077.1:p.Asp557Glu
NM_001164749.2:c.1977C>A MANE Select	NP_001158221.1:p.Asp659Glu
NM_001165893.2:c.1887C>A	NP_001159365.1:p.Asp629Glu
NM_022123.3:c.1881C>A	NP_071406.1:p.Asp627Glu
NM_173159.3:c.1938C>A	NP_775182.1:p.Asp646Glu
NM_001394988.1:c.1932C>A	NP_001381917.1:p.Asp644Glu
NM_001394989.1:c.1878C>A	NP_001381918.1:p.Asp626Glu