Canonical Allele Identifier: CA2128327122

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800227C= , CM000676.2:g.33800227C=	GRCh38
NC_000014.8:g.34269433C= , CM000676.1:g.34269433C=	GRCh37
NC_000014.7:g.33339184C=	NCBI36
NG_013036.1:g.865975C=
NG_013036.2:g.865975C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1920C= MANE Select	ENSP00000348460.4:p.Pro640=
ENST00000551634.6:c.1929C=	ENSP00000448373.2:p.Pro643=
ENST00000680362.1:c.1820C=
ENST00000681323.1:c.793+2646C=
ENST00000346562.6:c.1824C=	ENSP00000319610.5:p.Pro608=
ENST00000356141.8:c.1920C=	ENSP00000348460.4:p.Pro640=
ENST00000357798.9:c.1881C=	ENSP00000350446.5:p.Pro627=
ENST00000548645.5:c.1830C=	ENSP00000448916.1:p.Pro610=
ENST00000551492.5:c.1935C=	ENSP00000450392.1:p.Pro645=
ENST00000551634.5:c.1842C=	ENSP00000448373.1:p.Pro614=
NM_001164749.1:c.1920C=	NP_001158221.1:p.Pro640=
NM_001165893.1:c.1830C=	NP_001159365.1:p.Pro610=
NM_022123.2:c.1824C=	NP_071406.1:p.Pro608=
NM_173159.2:c.1881C=	NP_775182.1:p.Pro627=
XM_005267991.2:c.1941C=	XP_005268048.1:p.Pro647=
XM_005267992.2:c.1935C=	XP_005268049.1:p.Pro645=
XM_005267993.2:c.1881C=	XP_005268050.1:p.Pro627=
XM_011537067.1:c.1971C=	XP_011535369.1:p.Pro657=
XM_011537068.1:c.1962C=	XP_011535370.1:p.Pro654=
XM_011537069.1:c.1932C=	XP_011535371.1:p.Pro644=
XM_011537070.1:c.1875C=	XP_011535372.1:p.Pro625=
XM_011537071.1:c.1842C=	XP_011535373.1:p.Pro614=
XM_011537072.1:c.1821C=	XP_011535374.1:p.Pro607=
XM_011537073.1:c.1614C=	XP_011535375.1:p.Pro538=
XM_011537074.1:c.1614C=	XP_011535376.1:p.Pro538=
XM_005267991.3:c.2028C=	XP_005268048.2:p.Pro676=
XM_005267992.3:c.2022C=	XP_005268049.2:p.Pro674=
XM_011537067.2:c.1971C=	XP_011535369.1:p.Pro657=
XM_011537069.2:c.2019C=	XP_011535371.2:p.Pro673=
XM_011537070.2:c.1875C=	XP_011535372.1:p.Pro625=
XM_011537071.2:c.1929C=	XP_011535373.2:p.Pro643=
XM_011537072.2:c.1821C=	XP_011535374.1:p.Pro607=
XM_017021582.1:c.2079C=	XP_016877071.1:p.Pro693=
XM_017021583.1:c.2070C=	XP_016877072.1:p.Pro690=
XM_017021584.1:c.1989C=	XP_016877073.1:p.Pro663=
XM_017021585.1:c.1938C=	XP_016877074.1:p.Pro646=
XM_017021586.1:c.1614C=	XP_016877075.1:p.Pro538=
XM_017021587.1:c.1614C=	XP_016877076.1:p.Pro538=
XM_017021588.1:c.1614C=	XP_016877077.1:p.Pro538=
NM_001164749.2:c.1920C= MANE Select	NP_001158221.1:p.Pro640=
NM_001165893.2:c.1830C=	NP_001159365.1:p.Pro610=
NM_022123.3:c.1824C=	NP_071406.1:p.Pro608=
NM_173159.3:c.1881C=	NP_775182.1:p.Pro627=
NM_001394988.1:c.1875C=	NP_001381917.1:p.Pro625=
NM_001394989.1:c.1821C=	NP_001381918.1:p.Pro607=