Canonical Allele Identifier: CA389414114
Gene: NPAS3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.33800471G>C , CM000676.2:g.33800471G>C GRCh38
NC_000014.8:g.34269677G>C , CM000676.1:g.34269677G>C GRCh37
NC_000014.7:g.33339428G>C NCBI36
NG_013036.1:g.866219G>C
NG_013036.2:g.866219G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000356141.9:c.2164G>C MANE Select ENSP00000348460.4:p.Asp722His
ENST00000551634.6:c.2173G>C ENSP00000448373.2:p.Asp725His
ENST00000680362.1:c.2064G>C
ENST00000681323.1:c.793+2890G>C
ENST00000346562.6:c.2068G>C ENSP00000319610.5:p.Asp690His
ENST00000356141.8:c.2164G>C ENSP00000348460.4:p.Asp722His
ENST00000357798.9:c.2125G>C ENSP00000350446.5:p.Asp709His
ENST00000548645.5:c.2074G>C ENSP00000448916.1:p.Asp692His
ENST00000551492.5:c.2179G>C ENSP00000450392.1:p.Asp727His
ENST00000551634.5:c.2086G>C ENSP00000448373.1:p.Asp696His
NM_001164749.1:c.2164G>C NP_001158221.1:p.Asp722His
NM_001165893.1:c.2074G>C NP_001159365.1:p.Asp692His
NM_022123.2:c.2068G>C NP_071406.1:p.Asp690His
NM_173159.2:c.2125G>C NP_775182.1:p.Asp709His
XM_005267991.2:c.2185G>C XP_005268048.1:p.Asp729His
XM_005267992.2:c.2179G>C XP_005268049.1:p.Asp727His
XM_005267993.2:c.2125G>C XP_005268050.1:p.Asp709His
XM_011537067.1:c.2215G>C XP_011535369.1:p.Asp739His
XM_011537068.1:c.2206G>C XP_011535370.1:p.Asp736His
XM_011537069.1:c.2176G>C XP_011535371.1:p.Asp726His
XM_011537070.1:c.2119G>C XP_011535372.1:p.Asp707His
XM_011537071.1:c.2086G>C XP_011535373.1:p.Asp696His
XM_011537072.1:c.2065G>C XP_011535374.1:p.Asp689His
XM_011537073.1:c.1858G>C XP_011535375.1:p.Asp620His
XM_011537074.1:c.1858G>C XP_011535376.1:p.Asp620His
XM_005267991.3:c.2272G>C XP_005268048.2:p.Asp758His
XM_005267992.3:c.2266G>C XP_005268049.2:p.Asp756His
XM_011537067.2:c.2215G>C XP_011535369.1:p.Asp739His
XM_011537069.2:c.2263G>C XP_011535371.2:p.Asp755His
XM_011537070.2:c.2119G>C XP_011535372.1:p.Asp707His
XM_011537071.2:c.2173G>C XP_011535373.2:p.Asp725His
XM_011537072.2:c.2065G>C XP_011535374.1:p.Asp689His
XM_017021582.1:c.2323G>C XP_016877071.1:p.Asp775His
XM_017021583.1:c.2314G>C XP_016877072.1:p.Asp772His
XM_017021584.1:c.2233G>C XP_016877073.1:p.Asp745His
XM_017021585.1:c.2182G>C XP_016877074.1:p.Asp728His
XM_017021586.1:c.1858G>C XP_016877075.1:p.Asp620His
XM_017021587.1:c.1858G>C XP_016877076.1:p.Asp620His
XM_017021588.1:c.1858G>C XP_016877077.1:p.Asp620His
NM_001164749.2:c.2164G>C MANE Select NP_001158221.1:p.Asp722His
NM_001165893.2:c.2074G>C NP_001159365.1:p.Asp692His
NM_022123.3:c.2068G>C NP_071406.1:p.Asp690His
NM_173159.3:c.2125G>C NP_775182.1:p.Asp709His
NM_001394988.1:c.2119G>C NP_001381917.1:p.Asp707His
NM_001394989.1:c.2065G>C NP_001381918.1:p.Asp689His