Canonical Allele Identifier: CA389413277

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269474A>T (hg19) ; chr14:g.33800268A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800268A>T , CM000676.2:g.33800268A>T	GRCh38
NC_000014.8:g.34269474A>T , CM000676.1:g.34269474A>T	GRCh37
NC_000014.7:g.33339225A>T	NCBI36
NG_013036.1:g.866016A>T
NG_013036.2:g.866016A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1961A>T MANE Select	ENSP00000348460.4:p.Glu654Val
ENST00000551634.6:c.1970A>T	ENSP00000448373.2:p.Glu657Val
ENST00000680362.1:c.1861A>T
ENST00000681323.1:c.793+2687A>T
ENST00000346562.6:c.1865A>T	ENSP00000319610.5:p.Glu622Val
ENST00000356141.8:c.1961A>T	ENSP00000348460.4:p.Glu654Val
ENST00000357798.9:c.1922A>T	ENSP00000350446.5:p.Glu641Val
ENST00000548645.5:c.1871A>T	ENSP00000448916.1:p.Glu624Val
ENST00000551492.5:c.1976A>T	ENSP00000450392.1:p.Glu659Val
ENST00000551634.5:c.1883A>T	ENSP00000448373.1:p.Glu628Val
NM_001164749.1:c.1961A>T	NP_001158221.1:p.Glu654Val
NM_001165893.1:c.1871A>T	NP_001159365.1:p.Glu624Val
NM_022123.2:c.1865A>T	NP_071406.1:p.Glu622Val
NM_173159.2:c.1922A>T	NP_775182.1:p.Glu641Val
XM_005267991.2:c.1982A>T	XP_005268048.1:p.Glu661Val
XM_005267992.2:c.1976A>T	XP_005268049.1:p.Glu659Val
XM_005267993.2:c.1922A>T	XP_005268050.1:p.Glu641Val
XM_011537067.1:c.2012A>T	XP_011535369.1:p.Glu671Val
XM_011537068.1:c.2003A>T	XP_011535370.1:p.Glu668Val
XM_011537069.1:c.1973A>T	XP_011535371.1:p.Glu658Val
XM_011537070.1:c.1916A>T	XP_011535372.1:p.Glu639Val
XM_011537071.1:c.1883A>T	XP_011535373.1:p.Glu628Val
XM_011537072.1:c.1862A>T	XP_011535374.1:p.Glu621Val
XM_011537073.1:c.1655A>T	XP_011535375.1:p.Glu552Val
XM_011537074.1:c.1655A>T	XP_011535376.1:p.Glu552Val
XM_005267991.3:c.2069A>T	XP_005268048.2:p.Glu690Val
XM_005267992.3:c.2063A>T	XP_005268049.2:p.Glu688Val
XM_011537067.2:c.2012A>T	XP_011535369.1:p.Glu671Val
XM_011537069.2:c.2060A>T	XP_011535371.2:p.Glu687Val
XM_011537070.2:c.1916A>T	XP_011535372.1:p.Glu639Val
XM_011537071.2:c.1970A>T	XP_011535373.2:p.Glu657Val
XM_011537072.2:c.1862A>T	XP_011535374.1:p.Glu621Val
XM_017021582.1:c.2120A>T	XP_016877071.1:p.Glu707Val
XM_017021583.1:c.2111A>T	XP_016877072.1:p.Glu704Val
XM_017021584.1:c.2030A>T	XP_016877073.1:p.Glu677Val
XM_017021585.1:c.1979A>T	XP_016877074.1:p.Glu660Val
XM_017021586.1:c.1655A>T	XP_016877075.1:p.Glu552Val
XM_017021587.1:c.1655A>T	XP_016877076.1:p.Glu552Val
XM_017021588.1:c.1655A>T	XP_016877077.1:p.Glu552Val
NM_001164749.2:c.1961A>T MANE Select	NP_001158221.1:p.Glu654Val
NM_001165893.2:c.1871A>T	NP_001159365.1:p.Glu624Val
NM_022123.3:c.1865A>T	NP_071406.1:p.Glu622Val
NM_173159.3:c.1922A>T	NP_775182.1:p.Glu641Val
NM_001394988.1:c.1916A>T	NP_001381917.1:p.Glu639Val
NM_001394989.1:c.1862A>T	NP_001381918.1:p.Glu621Val