Canonical Allele Identifier: CA389414300
Gene: NPAS3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.33800564G>A , CM000676.2:g.33800564G>A GRCh38
NC_000014.8:g.34269770G>A , CM000676.1:g.34269770G>A GRCh37
NC_000014.7:g.33339521G>A NCBI36
NG_013036.1:g.866312G>A
NG_013036.2:g.866312G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356141.9:c.2257G>A MANE Select ENSP00000348460.4:p.Ala753Thr
ENST00000551634.6:c.2266G>A ENSP00000448373.2:p.Ala756Thr
ENST00000680362.1:c.2157G>A
ENST00000681323.1:c.793+2983G>A
ENST00000346562.6:c.2161G>A ENSP00000319610.5:p.Ala721Thr
ENST00000356141.8:c.2257G>A ENSP00000348460.4:p.Ala753Thr
ENST00000357798.9:c.2218G>A ENSP00000350446.5:p.Ala740Thr
ENST00000548645.5:c.2167G>A ENSP00000448916.1:p.Ala723Thr
ENST00000551492.5:c.2272G>A ENSP00000450392.1:p.Ala758Thr
ENST00000551634.5:c.2179G>A ENSP00000448373.1:p.Ala727Thr
NM_001164749.1:c.2257G>A NP_001158221.1:p.Ala753Thr
NM_001165893.1:c.2167G>A NP_001159365.1:p.Ala723Thr
NM_022123.2:c.2161G>A NP_071406.1:p.Ala721Thr
NM_173159.2:c.2218G>A NP_775182.1:p.Ala740Thr
XM_005267991.2:c.2278G>A XP_005268048.1:p.Ala760Thr
XM_005267992.2:c.2272G>A XP_005268049.1:p.Ala758Thr
XM_005267993.2:c.2218G>A XP_005268050.1:p.Ala740Thr
XM_011537067.1:c.2308G>A XP_011535369.1:p.Ala770Thr
XM_011537068.1:c.2299G>A XP_011535370.1:p.Ala767Thr
XM_011537069.1:c.2269G>A XP_011535371.1:p.Ala757Thr
XM_011537070.1:c.2212G>A XP_011535372.1:p.Ala738Thr
XM_011537071.1:c.2179G>A XP_011535373.1:p.Ala727Thr
XM_011537072.1:c.2158G>A XP_011535374.1:p.Ala720Thr
XM_011537073.1:c.1951G>A XP_011535375.1:p.Ala651Thr
XM_011537074.1:c.1951G>A XP_011535376.1:p.Ala651Thr
XM_005267991.3:c.2365G>A XP_005268048.2:p.Ala789Thr
XM_005267992.3:c.2359G>A XP_005268049.2:p.Ala787Thr
XM_011537067.2:c.2308G>A XP_011535369.1:p.Ala770Thr
XM_011537069.2:c.2356G>A XP_011535371.2:p.Ala786Thr
XM_011537070.2:c.2212G>A XP_011535372.1:p.Ala738Thr
XM_011537071.2:c.2266G>A XP_011535373.2:p.Ala756Thr
XM_011537072.2:c.2158G>A XP_011535374.1:p.Ala720Thr
XM_017021582.1:c.2416G>A XP_016877071.1:p.Ala806Thr
XM_017021583.1:c.2407G>A XP_016877072.1:p.Ala803Thr
XM_017021584.1:c.2326G>A XP_016877073.1:p.Ala776Thr
XM_017021585.1:c.2275G>A XP_016877074.1:p.Ala759Thr
XM_017021586.1:c.1951G>A XP_016877075.1:p.Ala651Thr
XM_017021587.1:c.1951G>A XP_016877076.1:p.Ala651Thr
XM_017021588.1:c.1951G>A XP_016877077.1:p.Ala651Thr
NM_001164749.2:c.2257G>A MANE Select NP_001158221.1:p.Ala753Thr
NM_001165893.2:c.2167G>A NP_001159365.1:p.Ala723Thr
NM_022123.3:c.2161G>A NP_071406.1:p.Ala721Thr
NM_173159.3:c.2218G>A NP_775182.1:p.Ala740Thr
NM_001394988.1:c.2212G>A NP_001381917.1:p.Ala738Thr
NM_001394989.1:c.2158G>A NP_001381918.1:p.Ala720Thr