Canonical Allele Identifier: CA2128326790

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800063G= , CM000676.2:g.33800063G=	GRCh38
NC_000014.8:g.34269269G= , CM000676.1:g.34269269G=	GRCh37
NC_000014.7:g.33339020G=	NCBI36
NG_013036.1:g.865811G=
NG_013036.2:g.865811G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1756G= MANE Select	ENSP00000348460.4:p.Ala586=
ENST00000551634.6:c.1765G=	ENSP00000448373.2:p.Ala589=
ENST00000680362.1:c.1656G=
ENST00000681323.1:c.793+2482G=
ENST00000346562.6:c.1660G=	ENSP00000319610.5:p.Ala554=
ENST00000356141.8:c.1756G=	ENSP00000348460.4:p.Ala586=
ENST00000357798.9:c.1717G=	ENSP00000350446.5:p.Ala573=
ENST00000548645.5:c.1666G=	ENSP00000448916.1:p.Ala556=
ENST00000551492.5:c.1771G=	ENSP00000450392.1:p.Ala591=
ENST00000551634.5:c.1678G=	ENSP00000448373.1:p.Ala560=
NM_001164749.1:c.1756G=	NP_001158221.1:p.Ala586=
NM_001165893.1:c.1666G=	NP_001159365.1:p.Ala556=
NM_022123.2:c.1660G=	NP_071406.1:p.Ala554=
NM_173159.2:c.1717G=	NP_775182.1:p.Ala573=
XM_005267991.2:c.1777G=	XP_005268048.1:p.Ala593=
XM_005267992.2:c.1771G=	XP_005268049.1:p.Ala591=
XM_005267993.2:c.1717G=	XP_005268050.1:p.Ala573=
XM_011537067.1:c.1807G=	XP_011535369.1:p.Ala603=
XM_011537068.1:c.1798G=	XP_011535370.1:p.Ala600=
XM_011537069.1:c.1768G=	XP_011535371.1:p.Ala590=
XM_011537070.1:c.1711G=	XP_011535372.1:p.Ala571=
XM_011537071.1:c.1678G=	XP_011535373.1:p.Ala560=
XM_011537072.1:c.1657G=	XP_011535374.1:p.Ala553=
XM_011537073.1:c.1450G=	XP_011535375.1:p.Ala484=
XM_011537074.1:c.1450G=	XP_011535376.1:p.Ala484=
XM_005267991.3:c.1864G=	XP_005268048.2:p.Ala622=
XM_005267992.3:c.1858G=	XP_005268049.2:p.Ala620=
XM_011537067.2:c.1807G=	XP_011535369.1:p.Ala603=
XM_011537069.2:c.1855G=	XP_011535371.2:p.Ala619=
XM_011537070.2:c.1711G=	XP_011535372.1:p.Ala571=
XM_011537071.2:c.1765G=	XP_011535373.2:p.Ala589=
XM_011537072.2:c.1657G=	XP_011535374.1:p.Ala553=
XM_017021582.1:c.1915G=	XP_016877071.1:p.Ala639=
XM_017021583.1:c.1906G=	XP_016877072.1:p.Ala636=
XM_017021584.1:c.1825G=	XP_016877073.1:p.Ala609=
XM_017021585.1:c.1774G=	XP_016877074.1:p.Ala592=
XM_017021586.1:c.1450G=	XP_016877075.1:p.Ala484=
XM_017021587.1:c.1450G=	XP_016877076.1:p.Ala484=
XM_017021588.1:c.1450G=	XP_016877077.1:p.Ala484=
NM_001164749.2:c.1756G= MANE Select	NP_001158221.1:p.Ala586=
NM_001165893.2:c.1666G=	NP_001159365.1:p.Ala556=
NM_022123.3:c.1660G=	NP_071406.1:p.Ala554=
NM_173159.3:c.1717G=	NP_775182.1:p.Ala573=
NM_001394988.1:c.1711G=	NP_001381917.1:p.Ala571=
NM_001394989.1:c.1657G=	NP_001381918.1:p.Ala553=