Canonical Allele Identifier: CA389414119

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269679C>G (hg19) ; chr14:g.33800473C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800473C>G , CM000676.2:g.33800473C>G	GRCh38
NC_000014.8:g.34269679C>G , CM000676.1:g.34269679C>G	GRCh37
NC_000014.7:g.33339430C>G	NCBI36
NG_013036.1:g.866221C>G
NG_013036.2:g.866221C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000356141.9:c.2166C>G MANE Select	ENSP00000348460.4:p.Asp722Glu
ENST00000551634.6:c.2175C>G	ENSP00000448373.2:p.Asp725Glu
ENST00000680362.1:c.2066C>G
ENST00000681323.1:c.793+2892C>G
ENST00000346562.6:c.2070C>G	ENSP00000319610.5:p.Asp690Glu
ENST00000356141.8:c.2166C>G	ENSP00000348460.4:p.Asp722Glu
ENST00000357798.9:c.2127C>G	ENSP00000350446.5:p.Asp709Glu
ENST00000548645.5:c.2076C>G	ENSP00000448916.1:p.Asp692Glu
ENST00000551492.5:c.2181C>G	ENSP00000450392.1:p.Asp727Glu
ENST00000551634.5:c.2088C>G	ENSP00000448373.1:p.Asp696Glu
NM_001164749.1:c.2166C>G	NP_001158221.1:p.Asp722Glu
NM_001165893.1:c.2076C>G	NP_001159365.1:p.Asp692Glu
NM_022123.2:c.2070C>G	NP_071406.1:p.Asp690Glu
NM_173159.2:c.2127C>G	NP_775182.1:p.Asp709Glu
XM_005267991.2:c.2187C>G	XP_005268048.1:p.Asp729Glu
XM_005267992.2:c.2181C>G	XP_005268049.1:p.Asp727Glu
XM_005267993.2:c.2127C>G	XP_005268050.1:p.Asp709Glu
XM_011537067.1:c.2217C>G	XP_011535369.1:p.Asp739Glu
XM_011537068.1:c.2208C>G	XP_011535370.1:p.Asp736Glu
XM_011537069.1:c.2178C>G	XP_011535371.1:p.Asp726Glu
XM_011537070.1:c.2121C>G	XP_011535372.1:p.Asp707Glu
XM_011537071.1:c.2088C>G	XP_011535373.1:p.Asp696Glu
XM_011537072.1:c.2067C>G	XP_011535374.1:p.Asp689Glu
XM_011537073.1:c.1860C>G	XP_011535375.1:p.Asp620Glu
XM_011537074.1:c.1860C>G	XP_011535376.1:p.Asp620Glu
XM_005267991.3:c.2274C>G	XP_005268048.2:p.Asp758Glu
XM_005267992.3:c.2268C>G	XP_005268049.2:p.Asp756Glu
XM_011537067.2:c.2217C>G	XP_011535369.1:p.Asp739Glu
XM_011537069.2:c.2265C>G	XP_011535371.2:p.Asp755Glu
XM_011537070.2:c.2121C>G	XP_011535372.1:p.Asp707Glu
XM_011537071.2:c.2175C>G	XP_011535373.2:p.Asp725Glu
XM_011537072.2:c.2067C>G	XP_011535374.1:p.Asp689Glu
XM_017021582.1:c.2325C>G	XP_016877071.1:p.Asp775Glu
XM_017021583.1:c.2316C>G	XP_016877072.1:p.Asp772Glu
XM_017021584.1:c.2235C>G	XP_016877073.1:p.Asp745Glu
XM_017021585.1:c.2184C>G	XP_016877074.1:p.Asp728Glu
XM_017021586.1:c.1860C>G	XP_016877075.1:p.Asp620Glu
XM_017021587.1:c.1860C>G	XP_016877076.1:p.Asp620Glu
XM_017021588.1:c.1860C>G	XP_016877077.1:p.Asp620Glu
NM_001164749.2:c.2166C>G MANE Select	NP_001158221.1:p.Asp722Glu
NM_001165893.2:c.2076C>G	NP_001159365.1:p.Asp692Glu
NM_022123.3:c.2070C>G	NP_071406.1:p.Asp690Glu
NM_173159.3:c.2127C>G	NP_775182.1:p.Asp709Glu
NM_001394988.1:c.2121C>G	NP_001381917.1:p.Asp707Glu
NM_001394989.1:c.2067C>G	NP_001381918.1:p.Asp689Glu