Canonical Allele Identifier: CA2128327060

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800198G= , CM000676.2:g.33800198G=	GRCh38
NC_000014.8:g.34269404G= , CM000676.1:g.34269404G=	GRCh37
NC_000014.7:g.33339155G=	NCBI36
NG_013036.1:g.865946G=
NG_013036.2:g.865946G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1891G= MANE Select	ENSP00000348460.4:p.Val631=
ENST00000551634.6:c.1900G=	ENSP00000448373.2:p.Val634=
ENST00000680362.1:c.1791G=
ENST00000681323.1:c.793+2617G=
ENST00000346562.6:c.1795G=	ENSP00000319610.5:p.Val599=
ENST00000356141.8:c.1891G=	ENSP00000348460.4:p.Val631=
ENST00000357798.9:c.1852G=	ENSP00000350446.5:p.Val618=
ENST00000548645.5:c.1801G=	ENSP00000448916.1:p.Val601=
ENST00000551492.5:c.1906G=	ENSP00000450392.1:p.Val636=
ENST00000551634.5:c.1813G=	ENSP00000448373.1:p.Val605=
NM_001164749.1:c.1891G=	NP_001158221.1:p.Val631=
NM_001165893.1:c.1801G=	NP_001159365.1:p.Val601=
NM_022123.2:c.1795G=	NP_071406.1:p.Val599=
NM_173159.2:c.1852G=	NP_775182.1:p.Val618=
XM_005267991.2:c.1912G=	XP_005268048.1:p.Val638=
XM_005267992.2:c.1906G=	XP_005268049.1:p.Val636=
XM_005267993.2:c.1852G=	XP_005268050.1:p.Val618=
XM_011537067.1:c.1942G=	XP_011535369.1:p.Val648=
XM_011537068.1:c.1933G=	XP_011535370.1:p.Val645=
XM_011537069.1:c.1903G=	XP_011535371.1:p.Val635=
XM_011537070.1:c.1846G=	XP_011535372.1:p.Val616=
XM_011537071.1:c.1813G=	XP_011535373.1:p.Val605=
XM_011537072.1:c.1792G=	XP_011535374.1:p.Val598=
XM_011537073.1:c.1585G=	XP_011535375.1:p.Val529=
XM_011537074.1:c.1585G=	XP_011535376.1:p.Val529=
XM_005267991.3:c.1999G=	XP_005268048.2:p.Val667=
XM_005267992.3:c.1993G=	XP_005268049.2:p.Val665=
XM_011537067.2:c.1942G=	XP_011535369.1:p.Val648=
XM_011537069.2:c.1990G=	XP_011535371.2:p.Val664=
XM_011537070.2:c.1846G=	XP_011535372.1:p.Val616=
XM_011537071.2:c.1900G=	XP_011535373.2:p.Val634=
XM_011537072.2:c.1792G=	XP_011535374.1:p.Val598=
XM_017021582.1:c.2050G=	XP_016877071.1:p.Val684=
XM_017021583.1:c.2041G=	XP_016877072.1:p.Val681=
XM_017021584.1:c.1960G=	XP_016877073.1:p.Val654=
XM_017021585.1:c.1909G=	XP_016877074.1:p.Val637=
XM_017021586.1:c.1585G=	XP_016877075.1:p.Val529=
XM_017021587.1:c.1585G=	XP_016877076.1:p.Val529=
XM_017021588.1:c.1585G=	XP_016877077.1:p.Val529=
NM_001164749.2:c.1891G= MANE Select	NP_001158221.1:p.Val631=
NM_001165893.2:c.1801G=	NP_001159365.1:p.Val601=
NM_022123.3:c.1795G=	NP_071406.1:p.Val599=
NM_173159.3:c.1852G=	NP_775182.1:p.Val618=
NM_001394988.1:c.1846G=	NP_001381917.1:p.Val616=
NM_001394989.1:c.1792G=	NP_001381918.1:p.Val598=