Canonical Allele Identifier: CA389414003
Gene: NPAS3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.33800431C>A , CM000676.2:g.33800431C>A GRCh38
NC_000014.8:g.34269637C>A , CM000676.1:g.34269637C>A GRCh37
NC_000014.7:g.33339388C>A NCBI36
NG_013036.1:g.866179C>A
NG_013036.2:g.866179C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356141.9:c.2124C>A MANE Select ENSP00000348460.4:p.His708Gln
ENST00000551634.6:c.2133C>A ENSP00000448373.2:p.His711Gln
ENST00000680362.1:c.2024C>A
ENST00000681323.1:c.793+2850C>A
ENST00000346562.6:c.2028C>A ENSP00000319610.5:p.His676Gln
ENST00000356141.8:c.2124C>A ENSP00000348460.4:p.His708Gln
ENST00000357798.9:c.2085C>A ENSP00000350446.5:p.His695Gln
ENST00000548645.5:c.2034C>A ENSP00000448916.1:p.His678Gln
ENST00000551492.5:c.2139C>A ENSP00000450392.1:p.His713Gln
ENST00000551634.5:c.2046C>A ENSP00000448373.1:p.His682Gln
NM_001164749.1:c.2124C>A NP_001158221.1:p.His708Gln
NM_001165893.1:c.2034C>A NP_001159365.1:p.His678Gln
NM_022123.2:c.2028C>A NP_071406.1:p.His676Gln
NM_173159.2:c.2085C>A NP_775182.1:p.His695Gln
XM_005267991.2:c.2145C>A XP_005268048.1:p.His715Gln
XM_005267992.2:c.2139C>A XP_005268049.1:p.His713Gln
XM_005267993.2:c.2085C>A XP_005268050.1:p.His695Gln
XM_011537067.1:c.2175C>A XP_011535369.1:p.His725Gln
XM_011537068.1:c.2166C>A XP_011535370.1:p.His722Gln
XM_011537069.1:c.2136C>A XP_011535371.1:p.His712Gln
XM_011537070.1:c.2079C>A XP_011535372.1:p.His693Gln
XM_011537071.1:c.2046C>A XP_011535373.1:p.His682Gln
XM_011537072.1:c.2025C>A XP_011535374.1:p.His675Gln
XM_011537073.1:c.1818C>A XP_011535375.1:p.His606Gln
XM_011537074.1:c.1818C>A XP_011535376.1:p.His606Gln
XM_005267991.3:c.2232C>A XP_005268048.2:p.His744Gln
XM_005267992.3:c.2226C>A XP_005268049.2:p.His742Gln
XM_011537067.2:c.2175C>A XP_011535369.1:p.His725Gln
XM_011537069.2:c.2223C>A XP_011535371.2:p.His741Gln
XM_011537070.2:c.2079C>A XP_011535372.1:p.His693Gln
XM_011537071.2:c.2133C>A XP_011535373.2:p.His711Gln
XM_011537072.2:c.2025C>A XP_011535374.1:p.His675Gln
XM_017021582.1:c.2283C>A XP_016877071.1:p.His761Gln
XM_017021583.1:c.2274C>A XP_016877072.1:p.His758Gln
XM_017021584.1:c.2193C>A XP_016877073.1:p.His731Gln
XM_017021585.1:c.2142C>A XP_016877074.1:p.His714Gln
XM_017021586.1:c.1818C>A XP_016877075.1:p.His606Gln
XM_017021587.1:c.1818C>A XP_016877076.1:p.His606Gln
XM_017021588.1:c.1818C>A XP_016877077.1:p.His606Gln
NM_001164749.2:c.2124C>A MANE Select NP_001158221.1:p.His708Gln
NM_001165893.2:c.2034C>A NP_001159365.1:p.His678Gln
NM_022123.3:c.2028C>A NP_071406.1:p.His676Gln
NM_173159.3:c.2085C>A NP_775182.1:p.His695Gln
NM_001394988.1:c.2079C>A NP_001381917.1:p.His693Gln
NM_001394989.1:c.2025C>A NP_001381918.1:p.His675Gln