Canonical Allele Identifier: CA2128326796
Gene: NPAS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.33800066G= , CM000676.2:g.33800066G= GRCh38
NC_000014.8:g.34269272G= , CM000676.1:g.34269272G= GRCh37
NC_000014.7:g.33339023G= NCBI36
NG_013036.1:g.865814G=
NG_013036.2:g.865814G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356141.9:c.1759G= MANE Select ENSP00000348460.4:p.Gly587=
ENST00000551634.6:c.1768G= ENSP00000448373.2:p.Gly590=
ENST00000680362.1:c.1659G=
ENST00000681323.1:c.793+2485G=
ENST00000346562.6:c.1663G= ENSP00000319610.5:p.Gly555=
ENST00000356141.8:c.1759G= ENSP00000348460.4:p.Gly587=
ENST00000357798.9:c.1720G= ENSP00000350446.5:p.Gly574=
ENST00000548645.5:c.1669G= ENSP00000448916.1:p.Gly557=
ENST00000551492.5:c.1774G= ENSP00000450392.1:p.Gly592=
ENST00000551634.5:c.1681G= ENSP00000448373.1:p.Gly561=
NM_001164749.1:c.1759G= NP_001158221.1:p.Gly587=
NM_001165893.1:c.1669G= NP_001159365.1:p.Gly557=
NM_022123.2:c.1663G= NP_071406.1:p.Gly555=
NM_173159.2:c.1720G= NP_775182.1:p.Gly574=
XM_005267991.2:c.1780G= XP_005268048.1:p.Gly594=
XM_005267992.2:c.1774G= XP_005268049.1:p.Gly592=
XM_005267993.2:c.1720G= XP_005268050.1:p.Gly574=
XM_011537067.1:c.1810G= XP_011535369.1:p.Gly604=
XM_011537068.1:c.1801G= XP_011535370.1:p.Gly601=
XM_011537069.1:c.1771G= XP_011535371.1:p.Gly591=
XM_011537070.1:c.1714G= XP_011535372.1:p.Gly572=
XM_011537071.1:c.1681G= XP_011535373.1:p.Gly561=
XM_011537072.1:c.1660G= XP_011535374.1:p.Gly554=
XM_011537073.1:c.1453G= XP_011535375.1:p.Gly485=
XM_011537074.1:c.1453G= XP_011535376.1:p.Gly485=
XM_005267991.3:c.1867G= XP_005268048.2:p.Gly623=
XM_005267992.3:c.1861G= XP_005268049.2:p.Gly621=
XM_011537067.2:c.1810G= XP_011535369.1:p.Gly604=
XM_011537069.2:c.1858G= XP_011535371.2:p.Gly620=
XM_011537070.2:c.1714G= XP_011535372.1:p.Gly572=
XM_011537071.2:c.1768G= XP_011535373.2:p.Gly590=
XM_011537072.2:c.1660G= XP_011535374.1:p.Gly554=
XM_017021582.1:c.1918G= XP_016877071.1:p.Gly640=
XM_017021583.1:c.1909G= XP_016877072.1:p.Gly637=
XM_017021584.1:c.1828G= XP_016877073.1:p.Gly610=
XM_017021585.1:c.1777G= XP_016877074.1:p.Gly593=
XM_017021586.1:c.1453G= XP_016877075.1:p.Gly485=
XM_017021587.1:c.1453G= XP_016877076.1:p.Gly485=
XM_017021588.1:c.1453G= XP_016877077.1:p.Gly485=
NM_001164749.2:c.1759G= MANE Select NP_001158221.1:p.Gly587=
NM_001165893.2:c.1669G= NP_001159365.1:p.Gly557=
NM_022123.3:c.1663G= NP_071406.1:p.Gly555=
NM_173159.3:c.1720G= NP_775182.1:p.Gly574=
NM_001394988.1:c.1714G= NP_001381917.1:p.Gly572=
NM_001394989.1:c.1660G= NP_001381918.1:p.Gly554=