Canonical Allele Identifier: CA389413421
Gene: NPAS3 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000356141.9:c.1991T>A MANE Select ENSP00000348460.4:p.Ile664Asn
ENST00000551634.6:c.2000T>A ENSP00000448373.2:p.Ile667Asn
ENST00000680362.1:c.1891T>A
ENST00000681323.1:c.793+2717T>A
ENST00000346562.6:c.1895T>A ENSP00000319610.5:p.Ile632Asn
ENST00000356141.8:c.1991T>A ENSP00000348460.4:p.Ile664Asn
ENST00000357798.9:c.1952T>A ENSP00000350446.5:p.Ile651Asn
ENST00000548645.5:c.1901T>A ENSP00000448916.1:p.Ile634Asn
ENST00000551492.5:c.2006T>A ENSP00000450392.1:p.Ile669Asn
ENST00000551634.5:c.1913T>A ENSP00000448373.1:p.Ile638Asn
NM_001164749.1:c.1991T>A NP_001158221.1:p.Ile664Asn
NM_001165893.1:c.1901T>A NP_001159365.1:p.Ile634Asn
NM_022123.2:c.1895T>A NP_071406.1:p.Ile632Asn
NM_173159.2:c.1952T>A NP_775182.1:p.Ile651Asn
XM_005267991.2:c.2012T>A XP_005268048.1:p.Ile671Asn
XM_005267992.2:c.2006T>A XP_005268049.1:p.Ile669Asn
XM_005267993.2:c.1952T>A XP_005268050.1:p.Ile651Asn
XM_011537067.1:c.2042T>A XP_011535369.1:p.Ile681Asn
XM_011537068.1:c.2033T>A XP_011535370.1:p.Ile678Asn
XM_011537069.1:c.2003T>A XP_011535371.1:p.Ile668Asn
XM_011537070.1:c.1946T>A XP_011535372.1:p.Ile649Asn
XM_011537071.1:c.1913T>A XP_011535373.1:p.Ile638Asn
XM_011537072.1:c.1892T>A XP_011535374.1:p.Ile631Asn
XM_011537073.1:c.1685T>A XP_011535375.1:p.Ile562Asn
XM_011537074.1:c.1685T>A XP_011535376.1:p.Ile562Asn
XM_005267991.3:c.2099T>A XP_005268048.2:p.Ile700Asn
XM_005267992.3:c.2093T>A XP_005268049.2:p.Ile698Asn
XM_011537067.2:c.2042T>A XP_011535369.1:p.Ile681Asn
XM_011537069.2:c.2090T>A XP_011535371.2:p.Ile697Asn
XM_011537070.2:c.1946T>A XP_011535372.1:p.Ile649Asn
XM_011537071.2:c.2000T>A XP_011535373.2:p.Ile667Asn
XM_011537072.2:c.1892T>A XP_011535374.1:p.Ile631Asn
XM_017021582.1:c.2150T>A XP_016877071.1:p.Ile717Asn
XM_017021583.1:c.2141T>A XP_016877072.1:p.Ile714Asn
XM_017021584.1:c.2060T>A XP_016877073.1:p.Ile687Asn
XM_017021585.1:c.2009T>A XP_016877074.1:p.Ile670Asn
XM_017021586.1:c.1685T>A XP_016877075.1:p.Ile562Asn
XM_017021587.1:c.1685T>A XP_016877076.1:p.Ile562Asn
XM_017021588.1:c.1685T>A XP_016877077.1:p.Ile562Asn
NM_001164749.2:c.1991T>A MANE Select NP_001158221.1:p.Ile664Asn
NM_001165893.2:c.1901T>A NP_001159365.1:p.Ile634Asn
NM_022123.3:c.1895T>A NP_071406.1:p.Ile632Asn
NM_173159.3:c.1952T>A NP_775182.1:p.Ile651Asn
NM_001394988.1:c.1946T>A NP_001381917.1:p.Ile649Asn
NM_001394989.1:c.1892T>A NP_001381918.1:p.Ile631Asn