Canonical Allele Identifier: CA2128328028

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800593_33800614delinsCGGCGGCGGGGGCGGGGGCGGG , CM000676.2:g.33800593_33800614delinsCGGCGGCGGGGGCGGGGGCGGG	GRCh38
NC_000014.8:g.34269799_34269820delinsCGGCGGCGGGGGCGGGGGCGGG , CM000676.1:g.34269799_34269820delinsCGGCGGCGGGGGCGGGGGCGGG	GRCh37
NC_000014.7:g.33339550_33339571delinsCGGCGGCGGGGGCGGGGGCGGG	NCBI36
NG_013036.1:g.866341_866362delinsCGGCGGCGGGGGCGGGGGCGGG
NG_013036.2:g.866341_866362delinsCGGCGGCGGGGGCGGGGGCGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2286_2307delinsCGGCGGCGGGGGCGGGGGCGGG MANE Select	ENSP00000348460.4:p.Asn762=
ENST00000551634.6:c.2295_2316delinsCGGCGGCGGGGGCGGGGGCGGG	ENSP00000448373.2:p.Asn765=
ENST00000680362.1:c.2186_2207delinsCGGCGGCGGGGGCGGGGGCGGG
ENST00000681323.1:c.793+3012_793+3033delinsCGGCGGCGGGGGCGGGGGCGGG
ENST00000346562.6:c.2190_2211delinsCGGCGGCGGGGGCGGGGGCGGG	ENSP00000319610.5:p.Asn730=
ENST00000356141.8:c.2286_2307delinsCGGCGGCGGGGGCGGGGGCGGG	ENSP00000348460.4:p.Asn762=
ENST00000357798.9:c.2247_2268delinsCGGCGGCGGGGGCGGGGGCGGG	ENSP00000350446.5:p.Asn749=
ENST00000548645.5:c.2196_2217delinsCGGCGGCGGGGGCGGGGGCGGG	ENSP00000448916.1:p.Asn732=
ENST00000551492.5:c.2301_2322delinsCGGCGGCGGGGGCGGGGGCGGG	ENSP00000450392.1:p.Asn767=
ENST00000551634.5:c.2208_2229delinsCGGCGGCGGGGGCGGGGGCGGG	ENSP00000448373.1:p.Asn736=
NM_001164749.1:c.2286_2307delinsCGGCGGCGGGGGCGGGGGCGGG	NP_001158221.1:p.Asn762=
NM_001165893.1:c.2196_2217delinsCGGCGGCGGGGGCGGGGGCGGG	NP_001159365.1:p.Asn732=
NM_022123.2:c.2190_2211delinsCGGCGGCGGGGGCGGGGGCGGG	NP_071406.1:p.Asn730=
NM_173159.2:c.2247_2268delinsCGGCGGCGGGGGCGGGGGCGGG	NP_775182.1:p.Asn749=
XM_005267991.2:c.2307_2328delinsCGGCGGCGGGGGCGGGGGCGGG	XP_005268048.1:p.Asn769=
XM_005267992.2:c.2301_2322delinsCGGCGGCGGGGGCGGGGGCGGG	XP_005268049.1:p.Asn767=
XM_005267993.2:c.2247_2268delinsCGGCGGCGGGGGCGGGGGCGGG	XP_005268050.1:p.Asn749=
XM_011537067.1:c.2337_2358delinsCGGCGGCGGGGGCGGGGGCGGG	XP_011535369.1:p.Asn779=
XM_011537068.1:c.2328_2349delinsCGGCGGCGGGGGCGGGGGCGGG	XP_011535370.1:p.Asn776=
XM_011537069.1:c.2298_2319delinsCGGCGGCGGGGGCGGGGGCGGG	XP_011535371.1:p.Asn766=
XM_011537070.1:c.2241_2262delinsCGGCGGCGGGGGCGGGGGCGGG	XP_011535372.1:p.Asn747=
XM_011537071.1:c.2208_2229delinsCGGCGGCGGGGGCGGGGGCGGG	XP_011535373.1:p.Asn736=
XM_011537072.1:c.2187_2208delinsCGGCGGCGGGGGCGGGGGCGGG	XP_011535374.1:p.Asn729=
XM_011537073.1:c.1980_2001delinsCGGCGGCGGGGGCGGGGGCGGG	XP_011535375.1:p.Asn660=
XM_011537074.1:c.1980_2001delinsCGGCGGCGGGGGCGGGGGCGGG	XP_011535376.1:p.Asn660=
XM_005267991.3:c.2394_2415delinsCGGCGGCGGGGGCGGGGGCGGG	XP_005268048.2:p.Asn798=
XM_005267992.3:c.2388_2409delinsCGGCGGCGGGGGCGGGGGCGGG	XP_005268049.2:p.Asn796=
XM_011537067.2:c.2337_2358delinsCGGCGGCGGGGGCGGGGGCGGG	XP_011535369.1:p.Asn779=
XM_011537069.2:c.2385_2406delinsCGGCGGCGGGGGCGGGGGCGGG	XP_011535371.2:p.Asn795=
XM_011537070.2:c.2241_2262delinsCGGCGGCGGGGGCGGGGGCGGG	XP_011535372.1:p.Asn747=
XM_011537071.2:c.2295_2316delinsCGGCGGCGGGGGCGGGGGCGGG	XP_011535373.2:p.Asn765=
XM_011537072.2:c.2187_2208delinsCGGCGGCGGGGGCGGGGGCGGG	XP_011535374.1:p.Asn729=
XM_017021582.1:c.2445_2466delinsCGGCGGCGGGGGCGGGGGCGGG	XP_016877071.1:p.Asn815=
XM_017021583.1:c.2436_2457delinsCGGCGGCGGGGGCGGGGGCGGG	XP_016877072.1:p.Asn812=
XM_017021584.1:c.2355_2376delinsCGGCGGCGGGGGCGGGGGCGGG	XP_016877073.1:p.Asn785=
XM_017021585.1:c.2304_2325delinsCGGCGGCGGGGGCGGGGGCGGG	XP_016877074.1:p.Asn768=
XM_017021586.1:c.1980_2001delinsCGGCGGCGGGGGCGGGGGCGGG	XP_016877075.1:p.Asn660=
XM_017021587.1:c.1980_2001delinsCGGCGGCGGGGGCGGGGGCGGG	XP_016877076.1:p.Asn660=
XM_017021588.1:c.1980_2001delinsCGGCGGCGGGGGCGGGGGCGGG	XP_016877077.1:p.Asn660=
NM_001164749.2:c.2286_2307delinsCGGCGGCGGGGGCGGGGGCGGG MANE Select	NP_001158221.1:p.Asn762=
NM_001165893.2:c.2196_2217delinsCGGCGGCGGGGGCGGGGGCGGG	NP_001159365.1:p.Asn732=
NM_022123.3:c.2190_2211delinsCGGCGGCGGGGGCGGGGGCGGG	NP_071406.1:p.Asn730=
NM_173159.3:c.2247_2268delinsCGGCGGCGGGGGCGGGGGCGGG	NP_775182.1:p.Asn749=
NM_001394988.1:c.2241_2262delinsCGGCGGCGGGGGCGGGGGCGGG	NP_001381917.1:p.Asn747=
NM_001394989.1:c.2187_2208delinsCGGCGGCGGGGGCGGGGGCGGG	NP_001381918.1:p.Asn729=