Canonical Allele Identifier: CA2128327187

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800262T= , CM000676.2:g.33800262T=	GRCh38
NC_000014.8:g.34269468T= , CM000676.1:g.34269468T=	GRCh37
NC_000014.7:g.33339219T=	NCBI36
NG_013036.1:g.866010T=
NG_013036.2:g.866010T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1955T= MANE Select	ENSP00000348460.4:p.Ile652=
ENST00000551634.6:c.1964T=	ENSP00000448373.2:p.Ile655=
ENST00000680362.1:c.1855T=
ENST00000681323.1:c.793+2681T=
ENST00000346562.6:c.1859T=	ENSP00000319610.5:p.Ile620=
ENST00000356141.8:c.1955T=	ENSP00000348460.4:p.Ile652=
ENST00000357798.9:c.1916T=	ENSP00000350446.5:p.Ile639=
ENST00000548645.5:c.1865T=	ENSP00000448916.1:p.Ile622=
ENST00000551492.5:c.1970T=	ENSP00000450392.1:p.Ile657=
ENST00000551634.5:c.1877T=	ENSP00000448373.1:p.Ile626=
NM_001164749.1:c.1955T=	NP_001158221.1:p.Ile652=
NM_001165893.1:c.1865T=	NP_001159365.1:p.Ile622=
NM_022123.2:c.1859T=	NP_071406.1:p.Ile620=
NM_173159.2:c.1916T=	NP_775182.1:p.Ile639=
XM_005267991.2:c.1976T=	XP_005268048.1:p.Ile659=
XM_005267992.2:c.1970T=	XP_005268049.1:p.Ile657=
XM_005267993.2:c.1916T=	XP_005268050.1:p.Ile639=
XM_011537067.1:c.2006T=	XP_011535369.1:p.Ile669=
XM_011537068.1:c.1997T=	XP_011535370.1:p.Ile666=
XM_011537069.1:c.1967T=	XP_011535371.1:p.Ile656=
XM_011537070.1:c.1910T=	XP_011535372.1:p.Ile637=
XM_011537071.1:c.1877T=	XP_011535373.1:p.Ile626=
XM_011537072.1:c.1856T=	XP_011535374.1:p.Ile619=
XM_011537073.1:c.1649T=	XP_011535375.1:p.Ile550=
XM_011537074.1:c.1649T=	XP_011535376.1:p.Ile550=
XM_005267991.3:c.2063T=	XP_005268048.2:p.Ile688=
XM_005267992.3:c.2057T=	XP_005268049.2:p.Ile686=
XM_011537067.2:c.2006T=	XP_011535369.1:p.Ile669=
XM_011537069.2:c.2054T=	XP_011535371.2:p.Ile685=
XM_011537070.2:c.1910T=	XP_011535372.1:p.Ile637=
XM_011537071.2:c.1964T=	XP_011535373.2:p.Ile655=
XM_011537072.2:c.1856T=	XP_011535374.1:p.Ile619=
XM_017021582.1:c.2114T=	XP_016877071.1:p.Ile705=
XM_017021583.1:c.2105T=	XP_016877072.1:p.Ile702=
XM_017021584.1:c.2024T=	XP_016877073.1:p.Ile675=
XM_017021585.1:c.1973T=	XP_016877074.1:p.Ile658=
XM_017021586.1:c.1649T=	XP_016877075.1:p.Ile550=
XM_017021587.1:c.1649T=	XP_016877076.1:p.Ile550=
XM_017021588.1:c.1649T=	XP_016877077.1:p.Ile550=
NM_001164749.2:c.1955T= MANE Select	NP_001158221.1:p.Ile652=
NM_001165893.2:c.1865T=	NP_001159365.1:p.Ile622=
NM_022123.3:c.1859T=	NP_071406.1:p.Ile620=
NM_173159.3:c.1916T=	NP_775182.1:p.Ile639=
NM_001394988.1:c.1910T=	NP_001381917.1:p.Ile637=
NM_001394989.1:c.1856T=	NP_001381918.1:p.Ile619=