Canonical Allele Identifier: CA2128326987

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800164C= , CM000676.2:g.33800164C=	GRCh38
NC_000014.8:g.34269370C= , CM000676.1:g.34269370C=	GRCh37
NC_000014.7:g.33339121C=	NCBI36
NG_013036.1:g.865912C=
NG_013036.2:g.865912C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1857C= MANE Select	ENSP00000348460.4:p.Ser619=
ENST00000551634.6:c.1866C=	ENSP00000448373.2:p.Ser622=
ENST00000680362.1:c.1757C=
ENST00000681323.1:c.793+2583C=
ENST00000346562.6:c.1761C=	ENSP00000319610.5:p.Ser587=
ENST00000356141.8:c.1857C=	ENSP00000348460.4:p.Ser619=
ENST00000357798.9:c.1818C=	ENSP00000350446.5:p.Ser606=
ENST00000548645.5:c.1767C=	ENSP00000448916.1:p.Ser589=
ENST00000551492.5:c.1872C=	ENSP00000450392.1:p.Ser624=
ENST00000551634.5:c.1779C=	ENSP00000448373.1:p.Ser593=
NM_001164749.1:c.1857C=	NP_001158221.1:p.Ser619=
NM_001165893.1:c.1767C=	NP_001159365.1:p.Ser589=
NM_022123.2:c.1761C=	NP_071406.1:p.Ser587=
NM_173159.2:c.1818C=	NP_775182.1:p.Ser606=
XM_005267991.2:c.1878C=	XP_005268048.1:p.Ser626=
XM_005267992.2:c.1872C=	XP_005268049.1:p.Ser624=
XM_005267993.2:c.1818C=	XP_005268050.1:p.Ser606=
XM_011537067.1:c.1908C=	XP_011535369.1:p.Ser636=
XM_011537068.1:c.1899C=	XP_011535370.1:p.Ser633=
XM_011537069.1:c.1869C=	XP_011535371.1:p.Ser623=
XM_011537070.1:c.1812C=	XP_011535372.1:p.Ser604=
XM_011537071.1:c.1779C=	XP_011535373.1:p.Ser593=
XM_011537072.1:c.1758C=	XP_011535374.1:p.Ser586=
XM_011537073.1:c.1551C=	XP_011535375.1:p.Ser517=
XM_011537074.1:c.1551C=	XP_011535376.1:p.Ser517=
XM_005267991.3:c.1965C=	XP_005268048.2:p.Ser655=
XM_005267992.3:c.1959C=	XP_005268049.2:p.Ser653=
XM_011537067.2:c.1908C=	XP_011535369.1:p.Ser636=
XM_011537069.2:c.1956C=	XP_011535371.2:p.Ser652=
XM_011537070.2:c.1812C=	XP_011535372.1:p.Ser604=
XM_011537071.2:c.1866C=	XP_011535373.2:p.Ser622=
XM_011537072.2:c.1758C=	XP_011535374.1:p.Ser586=
XM_017021582.1:c.2016C=	XP_016877071.1:p.Ser672=
XM_017021583.1:c.2007C=	XP_016877072.1:p.Ser669=
XM_017021584.1:c.1926C=	XP_016877073.1:p.Ser642=
XM_017021585.1:c.1875C=	XP_016877074.1:p.Ser625=
XM_017021586.1:c.1551C=	XP_016877075.1:p.Ser517=
XM_017021587.1:c.1551C=	XP_016877076.1:p.Ser517=
XM_017021588.1:c.1551C=	XP_016877077.1:p.Ser517=
NM_001164749.2:c.1857C= MANE Select	NP_001158221.1:p.Ser619=
NM_001165893.2:c.1767C=	NP_001159365.1:p.Ser589=
NM_022123.3:c.1761C=	NP_071406.1:p.Ser587=
NM_173159.3:c.1818C=	NP_775182.1:p.Ser606=
NM_001394988.1:c.1812C=	NP_001381917.1:p.Ser604=
NM_001394989.1:c.1758C=	NP_001381918.1:p.Ser586=