Canonical Allele Identifier: CA2128327043

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800191G= , CM000676.2:g.33800191G=	GRCh38
NC_000014.8:g.34269397G= , CM000676.1:g.34269397G=	GRCh37
NC_000014.7:g.33339148G=	NCBI36
NG_013036.1:g.865939G=
NG_013036.2:g.865939G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1884G= MANE Select	ENSP00000348460.4:p.Ala628=
ENST00000551634.6:c.1893G=	ENSP00000448373.2:p.Ala631=
ENST00000680362.1:c.1784G=
ENST00000681323.1:c.793+2610G=
ENST00000346562.6:c.1788G=	ENSP00000319610.5:p.Ala596=
ENST00000356141.8:c.1884G=	ENSP00000348460.4:p.Ala628=
ENST00000357798.9:c.1845G=	ENSP00000350446.5:p.Ala615=
ENST00000548645.5:c.1794G=	ENSP00000448916.1:p.Ala598=
ENST00000551492.5:c.1899G=	ENSP00000450392.1:p.Ala633=
ENST00000551634.5:c.1806G=	ENSP00000448373.1:p.Ala602=
NM_001164749.1:c.1884G=	NP_001158221.1:p.Ala628=
NM_001165893.1:c.1794G=	NP_001159365.1:p.Ala598=
NM_022123.2:c.1788G=	NP_071406.1:p.Ala596=
NM_173159.2:c.1845G=	NP_775182.1:p.Ala615=
XM_005267991.2:c.1905G=	XP_005268048.1:p.Ala635=
XM_005267992.2:c.1899G=	XP_005268049.1:p.Ala633=
XM_005267993.2:c.1845G=	XP_005268050.1:p.Ala615=
XM_011537067.1:c.1935G=	XP_011535369.1:p.Ala645=
XM_011537068.1:c.1926G=	XP_011535370.1:p.Ala642=
XM_011537069.1:c.1896G=	XP_011535371.1:p.Ala632=
XM_011537070.1:c.1839G=	XP_011535372.1:p.Ala613=
XM_011537071.1:c.1806G=	XP_011535373.1:p.Ala602=
XM_011537072.1:c.1785G=	XP_011535374.1:p.Ala595=
XM_011537073.1:c.1578G=	XP_011535375.1:p.Ala526=
XM_011537074.1:c.1578G=	XP_011535376.1:p.Ala526=
XM_005267991.3:c.1992G=	XP_005268048.2:p.Ala664=
XM_005267992.3:c.1986G=	XP_005268049.2:p.Ala662=
XM_011537067.2:c.1935G=	XP_011535369.1:p.Ala645=
XM_011537069.2:c.1983G=	XP_011535371.2:p.Ala661=
XM_011537070.2:c.1839G=	XP_011535372.1:p.Ala613=
XM_011537071.2:c.1893G=	XP_011535373.2:p.Ala631=
XM_011537072.2:c.1785G=	XP_011535374.1:p.Ala595=
XM_017021582.1:c.2043G=	XP_016877071.1:p.Ala681=
XM_017021583.1:c.2034G=	XP_016877072.1:p.Ala678=
XM_017021584.1:c.1953G=	XP_016877073.1:p.Ala651=
XM_017021585.1:c.1902G=	XP_016877074.1:p.Ala634=
XM_017021586.1:c.1578G=	XP_016877075.1:p.Ala526=
XM_017021587.1:c.1578G=	XP_016877076.1:p.Ala526=
XM_017021588.1:c.1578G=	XP_016877077.1:p.Ala526=
NM_001164749.2:c.1884G= MANE Select	NP_001158221.1:p.Ala628=
NM_001165893.2:c.1794G=	NP_001159365.1:p.Ala598=
NM_022123.3:c.1788G=	NP_071406.1:p.Ala596=
NM_173159.3:c.1845G=	NP_775182.1:p.Ala615=
NM_001394988.1:c.1839G=	NP_001381917.1:p.Ala613=
NM_001394989.1:c.1785G=	NP_001381918.1:p.Ala595=