Canonical Allele Identifier: CA2128327418
Gene: NPAS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.33800408_33800431delinsGGTGGCGGTGGCGGGGGGCTGCAC , CM000676.2:g.33800408_33800431delinsGGTGGCGGTGGCGGGGGGCTGCAC GRCh38
NC_000014.8:g.34269614_34269637delinsGGTGGCGGTGGCGGGGGGCTGCAC , CM000676.1:g.34269614_34269637delinsGGTGGCGGTGGCGGGGGGCTGCAC GRCh37
NC_000014.7:g.33339365_33339388delinsGGTGGCGGTGGCGGGGGGCTGCAC NCBI36
NG_013036.1:g.866156_866179delinsGGTGGCGGTGGCGGGGGGCTGCAC
NG_013036.2:g.866156_866179delinsGGTGGCGGTGGCGGGGGGCTGCAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000356141.9:c.2101_2124delinsGGTGGCGGTGGCGGGGGGCTGCAC MANE Select ENSP00000348460.4:p.Gly701=
ENST00000551634.6:c.2110_2133delinsGGTGGCGGTGGCGGGGGGCTGCAC ENSP00000448373.2:p.Gly704=
ENST00000680362.1:c.2001_2024delinsGGTGGCGGTGGCGGGGGGCTGCAC
ENST00000681323.1:c.793+2827_793+2850delinsGGTGGCGGTGGCGGGGGGCTGCAC
ENST00000346562.6:c.2005_2028delinsGGTGGCGGTGGCGGGGGGCTGCAC ENSP00000319610.5:p.Gly669=
ENST00000356141.8:c.2101_2124delinsGGTGGCGGTGGCGGGGGGCTGCAC ENSP00000348460.4:p.Gly701=
ENST00000357798.9:c.2062_2085delinsGGTGGCGGTGGCGGGGGGCTGCAC ENSP00000350446.5:p.Gly688=
ENST00000548645.5:c.2011_2034delinsGGTGGCGGTGGCGGGGGGCTGCAC ENSP00000448916.1:p.Gly671=
ENST00000551492.5:c.2116_2139delinsGGTGGCGGTGGCGGGGGGCTGCAC ENSP00000450392.1:p.Gly706=
ENST00000551634.5:c.2023_2046delinsGGTGGCGGTGGCGGGGGGCTGCAC ENSP00000448373.1:p.Gly675=
NM_001164749.1:c.2101_2124delinsGGTGGCGGTGGCGGGGGGCTGCAC NP_001158221.1:p.Gly701=
NM_001165893.1:c.2011_2034delinsGGTGGCGGTGGCGGGGGGCTGCAC NP_001159365.1:p.Gly671=
NM_022123.2:c.2005_2028delinsGGTGGCGGTGGCGGGGGGCTGCAC NP_071406.1:p.Gly669=
NM_173159.2:c.2062_2085delinsGGTGGCGGTGGCGGGGGGCTGCAC NP_775182.1:p.Gly688=
XM_005267991.2:c.2122_2145delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_005268048.1:p.Gly708=
XM_005267992.2:c.2116_2139delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_005268049.1:p.Gly706=
XM_005267993.2:c.2062_2085delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_005268050.1:p.Gly688=
XM_011537067.1:c.2152_2175delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_011535369.1:p.Gly718=
XM_011537068.1:c.2143_2166delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_011535370.1:p.Gly715=
XM_011537069.1:c.2113_2136delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_011535371.1:p.Gly705=
XM_011537070.1:c.2056_2079delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_011535372.1:p.Gly686=
XM_011537071.1:c.2023_2046delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_011535373.1:p.Gly675=
XM_011537072.1:c.2002_2025delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_011535374.1:p.Gly668=
XM_011537073.1:c.1795_1818delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_011535375.1:p.Gly599=
XM_011537074.1:c.1795_1818delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_011535376.1:p.Gly599=
XM_005267991.3:c.2209_2232delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_005268048.2:p.Gly737=
XM_005267992.3:c.2203_2226delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_005268049.2:p.Gly735=
XM_011537067.2:c.2152_2175delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_011535369.1:p.Gly718=
XM_011537069.2:c.2200_2223delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_011535371.2:p.Gly734=
XM_011537070.2:c.2056_2079delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_011535372.1:p.Gly686=
XM_011537071.2:c.2110_2133delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_011535373.2:p.Gly704=
XM_011537072.2:c.2002_2025delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_011535374.1:p.Gly668=
XM_017021582.1:c.2260_2283delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_016877071.1:p.Gly754=
XM_017021583.1:c.2251_2274delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_016877072.1:p.Gly751=
XM_017021584.1:c.2170_2193delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_016877073.1:p.Gly724=
XM_017021585.1:c.2119_2142delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_016877074.1:p.Gly707=
XM_017021586.1:c.1795_1818delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_016877075.1:p.Gly599=
XM_017021587.1:c.1795_1818delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_016877076.1:p.Gly599=
XM_017021588.1:c.1795_1818delinsGGTGGCGGTGGCGGGGGGCTGCAC XP_016877077.1:p.Gly599=
NM_001164749.2:c.2101_2124delinsGGTGGCGGTGGCGGGGGGCTGCAC MANE Select NP_001158221.1:p.Gly701=
NM_001165893.2:c.2011_2034delinsGGTGGCGGTGGCGGGGGGCTGCAC NP_001159365.1:p.Gly671=
NM_022123.3:c.2005_2028delinsGGTGGCGGTGGCGGGGGGCTGCAC NP_071406.1:p.Gly669=
NM_173159.3:c.2062_2085delinsGGTGGCGGTGGCGGGGGGCTGCAC NP_775182.1:p.Gly688=
NM_001394988.1:c.2056_2079delinsGGTGGCGGTGGCGGGGGGCTGCAC NP_001381917.1:p.Gly686=
NM_001394989.1:c.2002_2025delinsGGTGGCGGTGGCGGGGGGCTGCAC NP_001381918.1:p.Gly668=