Canonical Allele Identifier: CA389414154

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269696A>T (hg19) ; chr14:g.33800490A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800490A>T , CM000676.2:g.33800490A>T	GRCh38
NC_000014.8:g.34269696A>T , CM000676.1:g.34269696A>T	GRCh37
NC_000014.7:g.33339447A>T	NCBI36
NG_013036.1:g.866238A>T
NG_013036.2:g.866238A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2183A>T MANE Select	ENSP00000348460.4:p.Lys728Met
ENST00000551634.6:c.2192A>T	ENSP00000448373.2:p.Lys731Met
ENST00000680362.1:c.2083A>T
ENST00000681323.1:c.793+2909A>T
ENST00000346562.6:c.2087A>T	ENSP00000319610.5:p.Lys696Met
ENST00000356141.8:c.2183A>T	ENSP00000348460.4:p.Lys728Met
ENST00000357798.9:c.2144A>T	ENSP00000350446.5:p.Lys715Met
ENST00000548645.5:c.2093A>T	ENSP00000448916.1:p.Lys698Met
ENST00000551492.5:c.2198A>T	ENSP00000450392.1:p.Lys733Met
ENST00000551634.5:c.2105A>T	ENSP00000448373.1:p.Lys702Met
NM_001164749.1:c.2183A>T	NP_001158221.1:p.Lys728Met
NM_001165893.1:c.2093A>T	NP_001159365.1:p.Lys698Met
NM_022123.2:c.2087A>T	NP_071406.1:p.Lys696Met
NM_173159.2:c.2144A>T	NP_775182.1:p.Lys715Met
XM_005267991.2:c.2204A>T	XP_005268048.1:p.Lys735Met
XM_005267992.2:c.2198A>T	XP_005268049.1:p.Lys733Met
XM_005267993.2:c.2144A>T	XP_005268050.1:p.Lys715Met
XM_011537067.1:c.2234A>T	XP_011535369.1:p.Lys745Met
XM_011537068.1:c.2225A>T	XP_011535370.1:p.Lys742Met
XM_011537069.1:c.2195A>T	XP_011535371.1:p.Lys732Met
XM_011537070.1:c.2138A>T	XP_011535372.1:p.Lys713Met
XM_011537071.1:c.2105A>T	XP_011535373.1:p.Lys702Met
XM_011537072.1:c.2084A>T	XP_011535374.1:p.Lys695Met
XM_011537073.1:c.1877A>T	XP_011535375.1:p.Lys626Met
XM_011537074.1:c.1877A>T	XP_011535376.1:p.Lys626Met
XM_005267991.3:c.2291A>T	XP_005268048.2:p.Lys764Met
XM_005267992.3:c.2285A>T	XP_005268049.2:p.Lys762Met
XM_011537067.2:c.2234A>T	XP_011535369.1:p.Lys745Met
XM_011537069.2:c.2282A>T	XP_011535371.2:p.Lys761Met
XM_011537070.2:c.2138A>T	XP_011535372.1:p.Lys713Met
XM_011537071.2:c.2192A>T	XP_011535373.2:p.Lys731Met
XM_011537072.2:c.2084A>T	XP_011535374.1:p.Lys695Met
XM_017021582.1:c.2342A>T	XP_016877071.1:p.Lys781Met
XM_017021583.1:c.2333A>T	XP_016877072.1:p.Lys778Met
XM_017021584.1:c.2252A>T	XP_016877073.1:p.Lys751Met
XM_017021585.1:c.2201A>T	XP_016877074.1:p.Lys734Met
XM_017021586.1:c.1877A>T	XP_016877075.1:p.Lys626Met
XM_017021587.1:c.1877A>T	XP_016877076.1:p.Lys626Met
XM_017021588.1:c.1877A>T	XP_016877077.1:p.Lys626Met
NM_001164749.2:c.2183A>T MANE Select	NP_001158221.1:p.Lys728Met
NM_001165893.2:c.2093A>T	NP_001159365.1:p.Lys698Met
NM_022123.3:c.2087A>T	NP_071406.1:p.Lys696Met
NM_173159.3:c.2144A>T	NP_775182.1:p.Lys715Met
NM_001394988.1:c.2138A>T	NP_001381917.1:p.Lys713Met
NM_001394989.1:c.2084A>T	NP_001381918.1:p.Lys695Met