Canonical Allele Identifier: CA2128326854

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800086C= , CM000676.2:g.33800086C=	GRCh38
NC_000014.8:g.34269292C= , CM000676.1:g.34269292C=	GRCh37
NC_000014.7:g.33339043C=	NCBI36
NG_013036.1:g.865834C=
NG_013036.2:g.865834C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1779C= MANE Select	ENSP00000348460.4:p.Ala593=
ENST00000551634.6:c.1788C=	ENSP00000448373.2:p.Ala596=
ENST00000680362.1:c.1679C=
ENST00000681323.1:c.793+2505C=
ENST00000346562.6:c.1683C=	ENSP00000319610.5:p.Ala561=
ENST00000356141.8:c.1779C=	ENSP00000348460.4:p.Ala593=
ENST00000357798.9:c.1740C=	ENSP00000350446.5:p.Ala580=
ENST00000548645.5:c.1689C=	ENSP00000448916.1:p.Ala563=
ENST00000551492.5:c.1794C=	ENSP00000450392.1:p.Ala598=
ENST00000551634.5:c.1701C=	ENSP00000448373.1:p.Ala567=
NM_001164749.1:c.1779C=	NP_001158221.1:p.Ala593=
NM_001165893.1:c.1689C=	NP_001159365.1:p.Ala563=
NM_022123.2:c.1683C=	NP_071406.1:p.Ala561=
NM_173159.2:c.1740C=	NP_775182.1:p.Ala580=
XM_005267991.2:c.1800C=	XP_005268048.1:p.Ala600=
XM_005267992.2:c.1794C=	XP_005268049.1:p.Ala598=
XM_005267993.2:c.1740C=	XP_005268050.1:p.Ala580=
XM_011537067.1:c.1830C=	XP_011535369.1:p.Ala610=
XM_011537068.1:c.1821C=	XP_011535370.1:p.Ala607=
XM_011537069.1:c.1791C=	XP_011535371.1:p.Ala597=
XM_011537070.1:c.1734C=	XP_011535372.1:p.Ala578=
XM_011537071.1:c.1701C=	XP_011535373.1:p.Ala567=
XM_011537072.1:c.1680C=	XP_011535374.1:p.Ala560=
XM_011537073.1:c.1473C=	XP_011535375.1:p.Ala491=
XM_011537074.1:c.1473C=	XP_011535376.1:p.Ala491=
XM_005267991.3:c.1887C=	XP_005268048.2:p.Ala629=
XM_005267992.3:c.1881C=	XP_005268049.2:p.Ala627=
XM_011537067.2:c.1830C=	XP_011535369.1:p.Ala610=
XM_011537069.2:c.1878C=	XP_011535371.2:p.Ala626=
XM_011537070.2:c.1734C=	XP_011535372.1:p.Ala578=
XM_011537071.2:c.1788C=	XP_011535373.2:p.Ala596=
XM_011537072.2:c.1680C=	XP_011535374.1:p.Ala560=
XM_017021582.1:c.1938C=	XP_016877071.1:p.Ala646=
XM_017021583.1:c.1929C=	XP_016877072.1:p.Ala643=
XM_017021584.1:c.1848C=	XP_016877073.1:p.Ala616=
XM_017021585.1:c.1797C=	XP_016877074.1:p.Ala599=
XM_017021586.1:c.1473C=	XP_016877075.1:p.Ala491=
XM_017021587.1:c.1473C=	XP_016877076.1:p.Ala491=
XM_017021588.1:c.1473C=	XP_016877077.1:p.Ala491=
NM_001164749.2:c.1779C= MANE Select	NP_001158221.1:p.Ala593=
NM_001165893.2:c.1689C=	NP_001159365.1:p.Ala563=
NM_022123.3:c.1683C=	NP_071406.1:p.Ala561=
NM_173159.3:c.1740C=	NP_775182.1:p.Ala580=
NM_001394988.1:c.1734C=	NP_001381917.1:p.Ala578=
NM_001394989.1:c.1680C=	NP_001381918.1:p.Ala560=