Canonical Allele Identifier: CA2128326862
Gene: NPAS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.33800093A= , CM000676.2:g.33800093A= GRCh38
NC_000014.8:g.34269299A= , CM000676.1:g.34269299A= GRCh37
NC_000014.7:g.33339050A= NCBI36
NG_013036.1:g.865841A=
NG_013036.2:g.865841A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356141.9:c.1786A= MANE Select ENSP00000348460.4:p.Lys596=
ENST00000551634.6:c.1795A= ENSP00000448373.2:p.Lys599=
ENST00000680362.1:c.1686A=
ENST00000681323.1:c.793+2512A=
ENST00000346562.6:c.1690A= ENSP00000319610.5:p.Lys564=
ENST00000356141.8:c.1786A= ENSP00000348460.4:p.Lys596=
ENST00000357798.9:c.1747A= ENSP00000350446.5:p.Lys583=
ENST00000548645.5:c.1696A= ENSP00000448916.1:p.Lys566=
ENST00000551492.5:c.1801A= ENSP00000450392.1:p.Lys601=
ENST00000551634.5:c.1708A= ENSP00000448373.1:p.Lys570=
NM_001164749.1:c.1786A= NP_001158221.1:p.Lys596=
NM_001165893.1:c.1696A= NP_001159365.1:p.Lys566=
NM_022123.2:c.1690A= NP_071406.1:p.Lys564=
NM_173159.2:c.1747A= NP_775182.1:p.Lys583=
XM_005267991.2:c.1807A= XP_005268048.1:p.Lys603=
XM_005267992.2:c.1801A= XP_005268049.1:p.Lys601=
XM_005267993.2:c.1747A= XP_005268050.1:p.Lys583=
XM_011537067.1:c.1837A= XP_011535369.1:p.Lys613=
XM_011537068.1:c.1828A= XP_011535370.1:p.Lys610=
XM_011537069.1:c.1798A= XP_011535371.1:p.Lys600=
XM_011537070.1:c.1741A= XP_011535372.1:p.Lys581=
XM_011537071.1:c.1708A= XP_011535373.1:p.Lys570=
XM_011537072.1:c.1687A= XP_011535374.1:p.Lys563=
XM_011537073.1:c.1480A= XP_011535375.1:p.Lys494=
XM_011537074.1:c.1480A= XP_011535376.1:p.Lys494=
XM_005267991.3:c.1894A= XP_005268048.2:p.Lys632=
XM_005267992.3:c.1888A= XP_005268049.2:p.Lys630=
XM_011537067.2:c.1837A= XP_011535369.1:p.Lys613=
XM_011537069.2:c.1885A= XP_011535371.2:p.Lys629=
XM_011537070.2:c.1741A= XP_011535372.1:p.Lys581=
XM_011537071.2:c.1795A= XP_011535373.2:p.Lys599=
XM_011537072.2:c.1687A= XP_011535374.1:p.Lys563=
XM_017021582.1:c.1945A= XP_016877071.1:p.Lys649=
XM_017021583.1:c.1936A= XP_016877072.1:p.Lys646=
XM_017021584.1:c.1855A= XP_016877073.1:p.Lys619=
XM_017021585.1:c.1804A= XP_016877074.1:p.Lys602=
XM_017021586.1:c.1480A= XP_016877075.1:p.Lys494=
XM_017021587.1:c.1480A= XP_016877076.1:p.Lys494=
XM_017021588.1:c.1480A= XP_016877077.1:p.Lys494=
NM_001164749.2:c.1786A= MANE Select NP_001158221.1:p.Lys596=
NM_001165893.2:c.1696A= NP_001159365.1:p.Lys566=
NM_022123.3:c.1690A= NP_071406.1:p.Lys564=
NM_173159.3:c.1747A= NP_775182.1:p.Lys583=
NM_001394988.1:c.1741A= NP_001381917.1:p.Lys581=
NM_001394989.1:c.1687A= NP_001381918.1:p.Lys563=