Canonical Allele Identifier: CA2128327127

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800229A= , CM000676.2:g.33800229A=	GRCh38
NC_000014.8:g.34269435A= , CM000676.1:g.34269435A=	GRCh37
NC_000014.7:g.33339186A=	NCBI36
NG_013036.1:g.865977A=
NG_013036.2:g.865977A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1922A= MANE Select	ENSP00000348460.4:p.Asn641=
ENST00000551634.6:c.1931A=	ENSP00000448373.2:p.Asn644=
ENST00000680362.1:c.1822A=
ENST00000681323.1:c.793+2648A=
ENST00000346562.6:c.1826A=	ENSP00000319610.5:p.Asn609=
ENST00000356141.8:c.1922A=	ENSP00000348460.4:p.Asn641=
ENST00000357798.9:c.1883A=	ENSP00000350446.5:p.Asn628=
ENST00000548645.5:c.1832A=	ENSP00000448916.1:p.Asn611=
ENST00000551492.5:c.1937A=	ENSP00000450392.1:p.Asn646=
ENST00000551634.5:c.1844A=	ENSP00000448373.1:p.Asn615=
NM_001164749.1:c.1922A=	NP_001158221.1:p.Asn641=
NM_001165893.1:c.1832A=	NP_001159365.1:p.Asn611=
NM_022123.2:c.1826A=	NP_071406.1:p.Asn609=
NM_173159.2:c.1883A=	NP_775182.1:p.Asn628=
XM_005267991.2:c.1943A=	XP_005268048.1:p.Asn648=
XM_005267992.2:c.1937A=	XP_005268049.1:p.Asn646=
XM_005267993.2:c.1883A=	XP_005268050.1:p.Asn628=
XM_011537067.1:c.1973A=	XP_011535369.1:p.Asn658=
XM_011537068.1:c.1964A=	XP_011535370.1:p.Asn655=
XM_011537069.1:c.1934A=	XP_011535371.1:p.Asn645=
XM_011537070.1:c.1877A=	XP_011535372.1:p.Asn626=
XM_011537071.1:c.1844A=	XP_011535373.1:p.Asn615=
XM_011537072.1:c.1823A=	XP_011535374.1:p.Asn608=
XM_011537073.1:c.1616A=	XP_011535375.1:p.Asn539=
XM_011537074.1:c.1616A=	XP_011535376.1:p.Asn539=
XM_005267991.3:c.2030A=	XP_005268048.2:p.Asn677=
XM_005267992.3:c.2024A=	XP_005268049.2:p.Asn675=
XM_011537067.2:c.1973A=	XP_011535369.1:p.Asn658=
XM_011537069.2:c.2021A=	XP_011535371.2:p.Asn674=
XM_011537070.2:c.1877A=	XP_011535372.1:p.Asn626=
XM_011537071.2:c.1931A=	XP_011535373.2:p.Asn644=
XM_011537072.2:c.1823A=	XP_011535374.1:p.Asn608=
XM_017021582.1:c.2081A=	XP_016877071.1:p.Asn694=
XM_017021583.1:c.2072A=	XP_016877072.1:p.Asn691=
XM_017021584.1:c.1991A=	XP_016877073.1:p.Asn664=
XM_017021585.1:c.1940A=	XP_016877074.1:p.Asn647=
XM_017021586.1:c.1616A=	XP_016877075.1:p.Asn539=
XM_017021587.1:c.1616A=	XP_016877076.1:p.Asn539=
XM_017021588.1:c.1616A=	XP_016877077.1:p.Asn539=
NM_001164749.2:c.1922A= MANE Select	NP_001158221.1:p.Asn641=
NM_001165893.2:c.1832A=	NP_001159365.1:p.Asn611=
NM_022123.3:c.1826A=	NP_071406.1:p.Asn609=
NM_173159.3:c.1883A=	NP_775182.1:p.Asn628=
NM_001394988.1:c.1877A=	NP_001381917.1:p.Asn626=
NM_001394989.1:c.1823A=	NP_001381918.1:p.Asn608=