Canonical Allele Identifier: CA389413422
Gene: NPAS3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.33800298T>C , CM000676.2:g.33800298T>C GRCh38
NC_000014.8:g.34269504T>C , CM000676.1:g.34269504T>C GRCh37
NC_000014.7:g.33339255T>C NCBI36
NG_013036.1:g.866046T>C
NG_013036.2:g.866046T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356141.9:c.1991T>C MANE Select ENSP00000348460.4:p.Ile664Thr
ENST00000551634.6:c.2000T>C ENSP00000448373.2:p.Ile667Thr
ENST00000680362.1:c.1891T>C
ENST00000681323.1:c.793+2717T>C
ENST00000346562.6:c.1895T>C ENSP00000319610.5:p.Ile632Thr
ENST00000356141.8:c.1991T>C ENSP00000348460.4:p.Ile664Thr
ENST00000357798.9:c.1952T>C ENSP00000350446.5:p.Ile651Thr
ENST00000548645.5:c.1901T>C ENSP00000448916.1:p.Ile634Thr
ENST00000551492.5:c.2006T>C ENSP00000450392.1:p.Ile669Thr
ENST00000551634.5:c.1913T>C ENSP00000448373.1:p.Ile638Thr
NM_001164749.1:c.1991T>C NP_001158221.1:p.Ile664Thr
NM_001165893.1:c.1901T>C NP_001159365.1:p.Ile634Thr
NM_022123.2:c.1895T>C NP_071406.1:p.Ile632Thr
NM_173159.2:c.1952T>C NP_775182.1:p.Ile651Thr
XM_005267991.2:c.2012T>C XP_005268048.1:p.Ile671Thr
XM_005267992.2:c.2006T>C XP_005268049.1:p.Ile669Thr
XM_005267993.2:c.1952T>C XP_005268050.1:p.Ile651Thr
XM_011537067.1:c.2042T>C XP_011535369.1:p.Ile681Thr
XM_011537068.1:c.2033T>C XP_011535370.1:p.Ile678Thr
XM_011537069.1:c.2003T>C XP_011535371.1:p.Ile668Thr
XM_011537070.1:c.1946T>C XP_011535372.1:p.Ile649Thr
XM_011537071.1:c.1913T>C XP_011535373.1:p.Ile638Thr
XM_011537072.1:c.1892T>C XP_011535374.1:p.Ile631Thr
XM_011537073.1:c.1685T>C XP_011535375.1:p.Ile562Thr
XM_011537074.1:c.1685T>C XP_011535376.1:p.Ile562Thr
XM_005267991.3:c.2099T>C XP_005268048.2:p.Ile700Thr
XM_005267992.3:c.2093T>C XP_005268049.2:p.Ile698Thr
XM_011537067.2:c.2042T>C XP_011535369.1:p.Ile681Thr
XM_011537069.2:c.2090T>C XP_011535371.2:p.Ile697Thr
XM_011537070.2:c.1946T>C XP_011535372.1:p.Ile649Thr
XM_011537071.2:c.2000T>C XP_011535373.2:p.Ile667Thr
XM_011537072.2:c.1892T>C XP_011535374.1:p.Ile631Thr
XM_017021582.1:c.2150T>C XP_016877071.1:p.Ile717Thr
XM_017021583.1:c.2141T>C XP_016877072.1:p.Ile714Thr
XM_017021584.1:c.2060T>C XP_016877073.1:p.Ile687Thr
XM_017021585.1:c.2009T>C XP_016877074.1:p.Ile670Thr
XM_017021586.1:c.1685T>C XP_016877075.1:p.Ile562Thr
XM_017021587.1:c.1685T>C XP_016877076.1:p.Ile562Thr
XM_017021588.1:c.1685T>C XP_016877077.1:p.Ile562Thr
NM_001164749.2:c.1991T>C MANE Select NP_001158221.1:p.Ile664Thr
NM_001165893.2:c.1901T>C NP_001159365.1:p.Ile634Thr
NM_022123.3:c.1895T>C NP_071406.1:p.Ile632Thr
NM_173159.3:c.1952T>C NP_775182.1:p.Ile651Thr
NM_001394988.1:c.1946T>C NP_001381917.1:p.Ile649Thr
NM_001394989.1:c.1892T>C NP_001381918.1:p.Ile631Thr