Canonical Allele Identifier: CA389414327

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269783A>T (hg19) ; chr14:g.33800577A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800577A>T , CM000676.2:g.33800577A>T	GRCh38
NC_000014.8:g.34269783A>T , CM000676.1:g.34269783A>T	GRCh37
NC_000014.7:g.33339534A>T	NCBI36
NG_013036.1:g.866325A>T
NG_013036.2:g.866325A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000356141.9:c.2270A>T MANE Select	ENSP00000348460.4:p.Asp757Val
ENST00000551634.6:c.2279A>T	ENSP00000448373.2:p.Asp760Val
ENST00000680362.1:c.2170A>T
ENST00000681323.1:c.793+2996A>T
ENST00000346562.6:c.2174A>T	ENSP00000319610.5:p.Asp725Val
ENST00000356141.8:c.2270A>T	ENSP00000348460.4:p.Asp757Val
ENST00000357798.9:c.2231A>T	ENSP00000350446.5:p.Asp744Val
ENST00000548645.5:c.2180A>T	ENSP00000448916.1:p.Asp727Val
ENST00000551492.5:c.2285A>T	ENSP00000450392.1:p.Asp762Val
ENST00000551634.5:c.2192A>T	ENSP00000448373.1:p.Asp731Val
NM_001164749.1:c.2270A>T	NP_001158221.1:p.Asp757Val
NM_001165893.1:c.2180A>T	NP_001159365.1:p.Asp727Val
NM_022123.2:c.2174A>T	NP_071406.1:p.Asp725Val
NM_173159.2:c.2231A>T	NP_775182.1:p.Asp744Val
XM_005267991.2:c.2291A>T	XP_005268048.1:p.Asp764Val
XM_005267992.2:c.2285A>T	XP_005268049.1:p.Asp762Val
XM_005267993.2:c.2231A>T	XP_005268050.1:p.Asp744Val
XM_011537067.1:c.2321A>T	XP_011535369.1:p.Asp774Val
XM_011537068.1:c.2312A>T	XP_011535370.1:p.Asp771Val
XM_011537069.1:c.2282A>T	XP_011535371.1:p.Asp761Val
XM_011537070.1:c.2225A>T	XP_011535372.1:p.Asp742Val
XM_011537071.1:c.2192A>T	XP_011535373.1:p.Asp731Val
XM_011537072.1:c.2171A>T	XP_011535374.1:p.Asp724Val
XM_011537073.1:c.1964A>T	XP_011535375.1:p.Asp655Val
XM_011537074.1:c.1964A>T	XP_011535376.1:p.Asp655Val
XM_005267991.3:c.2378A>T	XP_005268048.2:p.Asp793Val
XM_005267992.3:c.2372A>T	XP_005268049.2:p.Asp791Val
XM_011537067.2:c.2321A>T	XP_011535369.1:p.Asp774Val
XM_011537069.2:c.2369A>T	XP_011535371.2:p.Asp790Val
XM_011537070.2:c.2225A>T	XP_011535372.1:p.Asp742Val
XM_011537071.2:c.2279A>T	XP_011535373.2:p.Asp760Val
XM_011537072.2:c.2171A>T	XP_011535374.1:p.Asp724Val
XM_017021582.1:c.2429A>T	XP_016877071.1:p.Asp810Val
XM_017021583.1:c.2420A>T	XP_016877072.1:p.Asp807Val
XM_017021584.1:c.2339A>T	XP_016877073.1:p.Asp780Val
XM_017021585.1:c.2288A>T	XP_016877074.1:p.Asp763Val
XM_017021586.1:c.1964A>T	XP_016877075.1:p.Asp655Val
XM_017021587.1:c.1964A>T	XP_016877076.1:p.Asp655Val
XM_017021588.1:c.1964A>T	XP_016877077.1:p.Asp655Val
NM_001164749.2:c.2270A>T MANE Select	NP_001158221.1:p.Asp757Val
NM_001165893.2:c.2180A>T	NP_001159365.1:p.Asp727Val
NM_022123.3:c.2174A>T	NP_071406.1:p.Asp725Val
NM_173159.3:c.2231A>T	NP_775182.1:p.Asp744Val
NM_001394988.1:c.2225A>T	NP_001381917.1:p.Asp742Val
NM_001394989.1:c.2171A>T	NP_001381918.1:p.Asp724Val