Canonical Allele Identifier: CA2128327366
Gene: NPAS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.33800396G= , CM000676.2:g.33800396G= GRCh38
NC_000014.8:g.34269602G= , CM000676.1:g.34269602G= GRCh37
NC_000014.7:g.33339353G= NCBI36
NG_013036.1:g.866144G=
NG_013036.2:g.866144G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356141.9:c.2089G= MANE Select ENSP00000348460.4:p.Gly697=
ENST00000551634.6:c.2098G= ENSP00000448373.2:p.Gly700=
ENST00000680362.1:c.1989G=
ENST00000681323.1:c.793+2815G=
ENST00000346562.6:c.1993G= ENSP00000319610.5:p.Gly665=
ENST00000356141.8:c.2089G= ENSP00000348460.4:p.Gly697=
ENST00000357798.9:c.2050G= ENSP00000350446.5:p.Gly684=
ENST00000548645.5:c.1999G= ENSP00000448916.1:p.Gly667=
ENST00000551492.5:c.2104G= ENSP00000450392.1:p.Gly702=
ENST00000551634.5:c.2011G= ENSP00000448373.1:p.Gly671=
NM_001164749.1:c.2089G= NP_001158221.1:p.Gly697=
NM_001165893.1:c.1999G= NP_001159365.1:p.Gly667=
NM_022123.2:c.1993G= NP_071406.1:p.Gly665=
NM_173159.2:c.2050G= NP_775182.1:p.Gly684=
XM_005267991.2:c.2110G= XP_005268048.1:p.Gly704=
XM_005267992.2:c.2104G= XP_005268049.1:p.Gly702=
XM_005267993.2:c.2050G= XP_005268050.1:p.Gly684=
XM_011537067.1:c.2140G= XP_011535369.1:p.Gly714=
XM_011537068.1:c.2131G= XP_011535370.1:p.Gly711=
XM_011537069.1:c.2101G= XP_011535371.1:p.Gly701=
XM_011537070.1:c.2044G= XP_011535372.1:p.Gly682=
XM_011537071.1:c.2011G= XP_011535373.1:p.Gly671=
XM_011537072.1:c.1990G= XP_011535374.1:p.Gly664=
XM_011537073.1:c.1783G= XP_011535375.1:p.Gly595=
XM_011537074.1:c.1783G= XP_011535376.1:p.Gly595=
XM_005267991.3:c.2197G= XP_005268048.2:p.Gly733=
XM_005267992.3:c.2191G= XP_005268049.2:p.Gly731=
XM_011537067.2:c.2140G= XP_011535369.1:p.Gly714=
XM_011537069.2:c.2188G= XP_011535371.2:p.Gly730=
XM_011537070.2:c.2044G= XP_011535372.1:p.Gly682=
XM_011537071.2:c.2098G= XP_011535373.2:p.Gly700=
XM_011537072.2:c.1990G= XP_011535374.1:p.Gly664=
XM_017021582.1:c.2248G= XP_016877071.1:p.Gly750=
XM_017021583.1:c.2239G= XP_016877072.1:p.Gly747=
XM_017021584.1:c.2158G= XP_016877073.1:p.Gly720=
XM_017021585.1:c.2107G= XP_016877074.1:p.Gly703=
XM_017021586.1:c.1783G= XP_016877075.1:p.Gly595=
XM_017021587.1:c.1783G= XP_016877076.1:p.Gly595=
XM_017021588.1:c.1783G= XP_016877077.1:p.Gly595=
NM_001164749.2:c.2089G= MANE Select NP_001158221.1:p.Gly697=
NM_001165893.2:c.1999G= NP_001159365.1:p.Gly667=
NM_022123.3:c.1993G= NP_071406.1:p.Gly665=
NM_173159.3:c.2050G= NP_775182.1:p.Gly684=
NM_001394988.1:c.2044G= NP_001381917.1:p.Gly682=
NM_001394989.1:c.1990G= NP_001381918.1:p.Gly664=