Canonical Allele Identifier: CA2801126439

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800478_33800479insCAC , CM000676.2:g.33800478_33800479insCAC	GRCh38
NC_000014.8:g.34269684_34269685insCAC , CM000676.1:g.34269684_34269685insCAC	GRCh37
NC_000014.7:g.33339435_33339436insCAC	NCBI36
NG_013036.1:g.866226_866227insCAC
NG_013036.2:g.866226_866227insCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2171_2172insCAC MANE Select	ENSP00000348460.4:p.Ala724_Ala725insThr
ENST00000551634.6:c.2180_2181insCAC	ENSP00000448373.2:p.Ala727_Ala728insThr
ENST00000680362.1:c.2071_2072insCAC
ENST00000681323.1:c.793+2897_793+2898insCAC
ENST00000346562.6:c.2075_2076insCAC	ENSP00000319610.5:p.Ala692_Ala693insThr
ENST00000356141.8:c.2171_2172insCAC	ENSP00000348460.4:p.Ala724_Ala725insThr
ENST00000357798.9:c.2132_2133insCAC	ENSP00000350446.5:p.Ala711_Ala712insThr
ENST00000548645.5:c.2081_2082insCAC	ENSP00000448916.1:p.Ala694_Ala695insThr
ENST00000551492.5:c.2186_2187insCAC	ENSP00000450392.1:p.Ala729_Ala730insThr
ENST00000551634.5:c.2093_2094insCAC	ENSP00000448373.1:p.Ala698_Ala699insThr
NM_001164749.1:c.2171_2172insCAC	NP_001158221.1:p.Ala724_Ala725insThr
NM_001165893.1:c.2081_2082insCAC	NP_001159365.1:p.Ala694_Ala695insThr
NM_022123.2:c.2075_2076insCAC	NP_071406.1:p.Ala692_Ala693insThr
NM_173159.2:c.2132_2133insCAC	NP_775182.1:p.Ala711_Ala712insThr
XM_005267991.2:c.2192_2193insCAC	XP_005268048.1:p.Ala731_Ala732insThr
XM_005267992.2:c.2186_2187insCAC	XP_005268049.1:p.Ala729_Ala730insThr
XM_005267993.2:c.2132_2133insCAC	XP_005268050.1:p.Ala711_Ala712insThr
XM_011537067.1:c.2222_2223insCAC	XP_011535369.1:p.Ala741_Ala742insThr
XM_011537068.1:c.2213_2214insCAC	XP_011535370.1:p.Ala738_Ala739insThr
XM_011537069.1:c.2183_2184insCAC	XP_011535371.1:p.Ala728_Ala729insThr
XM_011537070.1:c.2126_2127insCAC	XP_011535372.1:p.Ala709_Ala710insThr
XM_011537071.1:c.2093_2094insCAC	XP_011535373.1:p.Ala698_Ala699insThr
XM_011537072.1:c.2072_2073insCAC	XP_011535374.1:p.Ala691_Ala692insThr
XM_011537073.1:c.1865_1866insCAC	XP_011535375.1:p.Ala622_Ala623insThr
XM_011537074.1:c.1865_1866insCAC	XP_011535376.1:p.Ala622_Ala623insThr
XM_005267991.3:c.2279_2280insCAC	XP_005268048.2:p.Ala760_Ala761insThr
XM_005267992.3:c.2273_2274insCAC	XP_005268049.2:p.Ala758_Ala759insThr
XM_011537067.2:c.2222_2223insCAC	XP_011535369.1:p.Ala741_Ala742insThr
XM_011537069.2:c.2270_2271insCAC	XP_011535371.2:p.Ala757_Ala758insThr
XM_011537070.2:c.2126_2127insCAC	XP_011535372.1:p.Ala709_Ala710insThr
XM_011537071.2:c.2180_2181insCAC	XP_011535373.2:p.Ala727_Ala728insThr
XM_011537072.2:c.2072_2073insCAC	XP_011535374.1:p.Ala691_Ala692insThr
XM_017021582.1:c.2330_2331insCAC	XP_016877071.1:p.Ala777_Ala778insThr
XM_017021583.1:c.2321_2322insCAC	XP_016877072.1:p.Ala774_Ala775insThr
XM_017021584.1:c.2240_2241insCAC	XP_016877073.1:p.Ala747_Ala748insThr
XM_017021585.1:c.2189_2190insCAC	XP_016877074.1:p.Ala730_Ala731insThr
XM_017021586.1:c.1865_1866insCAC	XP_016877075.1:p.Ala622_Ala623insThr
XM_017021587.1:c.1865_1866insCAC	XP_016877076.1:p.Ala622_Ala623insThr
XM_017021588.1:c.1865_1866insCAC	XP_016877077.1:p.Ala622_Ala623insThr
NM_001164749.2:c.2171_2172insCAC MANE Select	NP_001158221.1:p.Ala724_Ala725insThr
NM_001165893.2:c.2081_2082insCAC	NP_001159365.1:p.Ala694_Ala695insThr
NM_022123.3:c.2075_2076insCAC	NP_071406.1:p.Ala692_Ala693insThr
NM_173159.3:c.2132_2133insCAC	NP_775182.1:p.Ala711_Ala712insThr
NM_001394988.1:c.2126_2127insCAC	NP_001381917.1:p.Ala709_Ala710insThr
NM_001394989.1:c.2072_2073insCAC	NP_001381918.1:p.Ala691_Ala692insThr