Canonical Allele Identifier: CA2562813026

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800486_33800487insCGCG , CM000676.2:g.33800486_33800487insCGCG	GRCh38
NC_000014.8:g.34269692_34269693insCGCG , CM000676.1:g.34269692_34269693insCGCG	GRCh37
NC_000014.7:g.33339443_33339444insCGCG	NCBI36
NG_013036.1:g.866234_866235insCGCG
NG_013036.2:g.866234_866235insCGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2179_2180insCGCG MANE Select	ENSP00000348460.4:p.Arg727ProfsTer?
ENST00000551634.6:c.2188_2189insCGCG	ENSP00000448373.2:p.Arg730ProfsTer?
ENST00000680362.1:c.2079_2080insCGCG
ENST00000681323.1:c.793+2905_793+2906insCGCG
ENST00000346562.6:c.2083_2084insCGCG	ENSP00000319610.5:p.Arg695ProfsTer?
ENST00000356141.8:c.2179_2180insCGCG	ENSP00000348460.4:p.Arg727ProfsTer?
ENST00000357798.9:c.2140_2141insCGCG	ENSP00000350446.5:p.Arg714ProfsTer?
ENST00000548645.5:c.2089_2090insCGCG	ENSP00000448916.1:p.Arg697ProfsTer?
ENST00000551492.5:c.2194_2195insCGCG	ENSP00000450392.1:p.Arg732ProfsTer?
ENST00000551634.5:c.2101_2102insCGCG	ENSP00000448373.1:p.Arg701ProfsTer?
NM_001164749.1:c.2179_2180insCGCG	NP_001158221.1:p.Arg727ProfsTer?
NM_001165893.1:c.2089_2090insCGCG	NP_001159365.1:p.Arg697ProfsTer?
NM_022123.2:c.2083_2084insCGCG	NP_071406.1:p.Arg695ProfsTer?
NM_173159.2:c.2140_2141insCGCG	NP_775182.1:p.Arg714ProfsTer?
XM_005267991.2:c.2200_2201insCGCG	XP_005268048.1:p.Arg734ProfsTer?
XM_005267992.2:c.2194_2195insCGCG	XP_005268049.1:p.Arg732ProfsTer?
XM_005267993.2:c.2140_2141insCGCG	XP_005268050.1:p.Arg714ProfsTer?
XM_011537067.1:c.2230_2231insCGCG	XP_011535369.1:p.Arg744ProfsTer?
XM_011537068.1:c.2221_2222insCGCG	XP_011535370.1:p.Arg741ProfsTer?
XM_011537069.1:c.2191_2192insCGCG	XP_011535371.1:p.Arg731ProfsTer?
XM_011537070.1:c.2134_2135insCGCG	XP_011535372.1:p.Arg712ProfsTer?
XM_011537071.1:c.2101_2102insCGCG	XP_011535373.1:p.Arg701ProfsTer?
XM_011537072.1:c.2080_2081insCGCG	XP_011535374.1:p.Arg694ProfsTer?
XM_011537073.1:c.1873_1874insCGCG	XP_011535375.1:p.Arg625ProfsTer?
XM_011537074.1:c.1873_1874insCGCG	XP_011535376.1:p.Arg625ProfsTer?
XM_005267991.3:c.2287_2288insCGCG	XP_005268048.2:p.Arg763ProfsTer?
XM_005267992.3:c.2281_2282insCGCG	XP_005268049.2:p.Arg761ProfsTer?
XM_011537067.2:c.2230_2231insCGCG	XP_011535369.1:p.Arg744ProfsTer?
XM_011537069.2:c.2278_2279insCGCG	XP_011535371.2:p.Arg760ProfsTer?
XM_011537070.2:c.2134_2135insCGCG	XP_011535372.1:p.Arg712ProfsTer?
XM_011537071.2:c.2188_2189insCGCG	XP_011535373.2:p.Arg730ProfsTer?
XM_011537072.2:c.2080_2081insCGCG	XP_011535374.1:p.Arg694ProfsTer?
XM_017021582.1:c.2338_2339insCGCG	XP_016877071.1:p.Arg780ProfsTer?
XM_017021583.1:c.2329_2330insCGCG	XP_016877072.1:p.Arg777ProfsTer?
XM_017021584.1:c.2248_2249insCGCG	XP_016877073.1:p.Arg750ProfsTer?
XM_017021585.1:c.2197_2198insCGCG	XP_016877074.1:p.Arg733ProfsTer?
XM_017021586.1:c.1873_1874insCGCG	XP_016877075.1:p.Arg625ProfsTer?
XM_017021587.1:c.1873_1874insCGCG	XP_016877076.1:p.Arg625ProfsTer?
XM_017021588.1:c.1873_1874insCGCG	XP_016877077.1:p.Arg625ProfsTer?
NM_001164749.2:c.2179_2180insCGCG MANE Select	NP_001158221.1:p.Arg727ProfsTer?
NM_001165893.2:c.2089_2090insCGCG	NP_001159365.1:p.Arg697ProfsTer?
NM_022123.3:c.2083_2084insCGCG	NP_071406.1:p.Arg695ProfsTer?
NM_173159.3:c.2140_2141insCGCG	NP_775182.1:p.Arg714ProfsTer?
NM_001394988.1:c.2134_2135insCGCG	NP_001381917.1:p.Arg712ProfsTer?
NM_001394989.1:c.2080_2081insCGCG	NP_001381918.1:p.Arg694ProfsTer?