Canonical Allele Identifier: CA2128327617

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800492A= , CM000676.2:g.33800492A=	GRCh38
NC_000014.8:g.34269698A= , CM000676.1:g.34269698A=	GRCh37
NC_000014.7:g.33339449A=	NCBI36
NG_013036.1:g.866240A=
NG_013036.2:g.866240A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2185A= MANE Select	ENSP00000348460.4:p.Thr729=
ENST00000551634.6:c.2194A=	ENSP00000448373.2:p.Thr732=
ENST00000680362.1:c.2085A=
ENST00000681323.1:c.793+2911A=
ENST00000346562.6:c.2089A=	ENSP00000319610.5:p.Thr697=
ENST00000356141.8:c.2185A=	ENSP00000348460.4:p.Thr729=
ENST00000357798.9:c.2146A=	ENSP00000350446.5:p.Thr716=
ENST00000548645.5:c.2095A=	ENSP00000448916.1:p.Thr699=
ENST00000551492.5:c.2200A=	ENSP00000450392.1:p.Thr734=
ENST00000551634.5:c.2107A=	ENSP00000448373.1:p.Thr703=
NM_001164749.1:c.2185A=	NP_001158221.1:p.Thr729=
NM_001165893.1:c.2095A=	NP_001159365.1:p.Thr699=
NM_022123.2:c.2089A=	NP_071406.1:p.Thr697=
NM_173159.2:c.2146A=	NP_775182.1:p.Thr716=
XM_005267991.2:c.2206A=	XP_005268048.1:p.Thr736=
XM_005267992.2:c.2200A=	XP_005268049.1:p.Thr734=
XM_005267993.2:c.2146A=	XP_005268050.1:p.Thr716=
XM_011537067.1:c.2236A=	XP_011535369.1:p.Thr746=
XM_011537068.1:c.2227A=	XP_011535370.1:p.Thr743=
XM_011537069.1:c.2197A=	XP_011535371.1:p.Thr733=
XM_011537070.1:c.2140A=	XP_011535372.1:p.Thr714=
XM_011537071.1:c.2107A=	XP_011535373.1:p.Thr703=
XM_011537072.1:c.2086A=	XP_011535374.1:p.Thr696=
XM_011537073.1:c.1879A=	XP_011535375.1:p.Thr627=
XM_011537074.1:c.1879A=	XP_011535376.1:p.Thr627=
XM_005267991.3:c.2293A=	XP_005268048.2:p.Thr765=
XM_005267992.3:c.2287A=	XP_005268049.2:p.Thr763=
XM_011537067.2:c.2236A=	XP_011535369.1:p.Thr746=
XM_011537069.2:c.2284A=	XP_011535371.2:p.Thr762=
XM_011537070.2:c.2140A=	XP_011535372.1:p.Thr714=
XM_011537071.2:c.2194A=	XP_011535373.2:p.Thr732=
XM_011537072.2:c.2086A=	XP_011535374.1:p.Thr696=
XM_017021582.1:c.2344A=	XP_016877071.1:p.Thr782=
XM_017021583.1:c.2335A=	XP_016877072.1:p.Thr779=
XM_017021584.1:c.2254A=	XP_016877073.1:p.Thr752=
XM_017021585.1:c.2203A=	XP_016877074.1:p.Thr735=
XM_017021586.1:c.1879A=	XP_016877075.1:p.Thr627=
XM_017021587.1:c.1879A=	XP_016877076.1:p.Thr627=
XM_017021588.1:c.1879A=	XP_016877077.1:p.Thr627=
NM_001164749.2:c.2185A= MANE Select	NP_001158221.1:p.Thr729=
NM_001165893.2:c.2095A=	NP_001159365.1:p.Thr699=
NM_022123.3:c.2089A=	NP_071406.1:p.Thr697=
NM_173159.3:c.2146A=	NP_775182.1:p.Thr716=
NM_001394988.1:c.2140A=	NP_001381917.1:p.Thr714=
NM_001394989.1:c.2086A=	NP_001381918.1:p.Thr696=