Canonical Allele Identifier: CA2128326996

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800165G= , CM000676.2:g.33800165G=	GRCh38
NC_000014.8:g.34269371G= , CM000676.1:g.34269371G=	GRCh37
NC_000014.7:g.33339122G=	NCBI36
NG_013036.1:g.865913G=
NG_013036.2:g.865913G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1858G= MANE Select	ENSP00000348460.4:p.Ala620=
ENST00000551634.6:c.1867G=	ENSP00000448373.2:p.Ala623=
ENST00000680362.1:c.1758G=
ENST00000681323.1:c.793+2584G=
ENST00000346562.6:c.1762G=	ENSP00000319610.5:p.Ala588=
ENST00000356141.8:c.1858G=	ENSP00000348460.4:p.Ala620=
ENST00000357798.9:c.1819G=	ENSP00000350446.5:p.Ala607=
ENST00000548645.5:c.1768G=	ENSP00000448916.1:p.Ala590=
ENST00000551492.5:c.1873G=	ENSP00000450392.1:p.Ala625=
ENST00000551634.5:c.1780G=	ENSP00000448373.1:p.Ala594=
NM_001164749.1:c.1858G=	NP_001158221.1:p.Ala620=
NM_001165893.1:c.1768G=	NP_001159365.1:p.Ala590=
NM_022123.2:c.1762G=	NP_071406.1:p.Ala588=
NM_173159.2:c.1819G=	NP_775182.1:p.Ala607=
XM_005267991.2:c.1879G=	XP_005268048.1:p.Ala627=
XM_005267992.2:c.1873G=	XP_005268049.1:p.Ala625=
XM_005267993.2:c.1819G=	XP_005268050.1:p.Ala607=
XM_011537067.1:c.1909G=	XP_011535369.1:p.Ala637=
XM_011537068.1:c.1900G=	XP_011535370.1:p.Ala634=
XM_011537069.1:c.1870G=	XP_011535371.1:p.Ala624=
XM_011537070.1:c.1813G=	XP_011535372.1:p.Ala605=
XM_011537071.1:c.1780G=	XP_011535373.1:p.Ala594=
XM_011537072.1:c.1759G=	XP_011535374.1:p.Ala587=
XM_011537073.1:c.1552G=	XP_011535375.1:p.Ala518=
XM_011537074.1:c.1552G=	XP_011535376.1:p.Ala518=
XM_005267991.3:c.1966G=	XP_005268048.2:p.Ala656=
XM_005267992.3:c.1960G=	XP_005268049.2:p.Ala654=
XM_011537067.2:c.1909G=	XP_011535369.1:p.Ala637=
XM_011537069.2:c.1957G=	XP_011535371.2:p.Ala653=
XM_011537070.2:c.1813G=	XP_011535372.1:p.Ala605=
XM_011537071.2:c.1867G=	XP_011535373.2:p.Ala623=
XM_011537072.2:c.1759G=	XP_011535374.1:p.Ala587=
XM_017021582.1:c.2017G=	XP_016877071.1:p.Ala673=
XM_017021583.1:c.2008G=	XP_016877072.1:p.Ala670=
XM_017021584.1:c.1927G=	XP_016877073.1:p.Ala643=
XM_017021585.1:c.1876G=	XP_016877074.1:p.Ala626=
XM_017021586.1:c.1552G=	XP_016877075.1:p.Ala518=
XM_017021587.1:c.1552G=	XP_016877076.1:p.Ala518=
XM_017021588.1:c.1552G=	XP_016877077.1:p.Ala518=
NM_001164749.2:c.1858G= MANE Select	NP_001158221.1:p.Ala620=
NM_001165893.2:c.1768G=	NP_001159365.1:p.Ala590=
NM_022123.3:c.1762G=	NP_071406.1:p.Ala588=
NM_173159.3:c.1819G=	NP_775182.1:p.Ala607=
NM_001394988.1:c.1813G=	NP_001381917.1:p.Ala605=
NM_001394989.1:c.1759G=	NP_001381918.1:p.Ala587=