Canonical Allele Identifier: CA2128327139

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800238C= , CM000676.2:g.33800238C=	GRCh38
NC_000014.8:g.34269444C= , CM000676.1:g.34269444C=	GRCh37
NC_000014.7:g.33339195C=	NCBI36
NG_013036.1:g.865986C=
NG_013036.2:g.865986C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1931C= MANE Select	ENSP00000348460.4:p.Ser644=
ENST00000551634.6:c.1940C=	ENSP00000448373.2:p.Ser647=
ENST00000680362.1:c.1831C=
ENST00000681323.1:c.793+2657C=
ENST00000346562.6:c.1835C=	ENSP00000319610.5:p.Ser612=
ENST00000356141.8:c.1931C=	ENSP00000348460.4:p.Ser644=
ENST00000357798.9:c.1892C=	ENSP00000350446.5:p.Ser631=
ENST00000548645.5:c.1841C=	ENSP00000448916.1:p.Ser614=
ENST00000551492.5:c.1946C=	ENSP00000450392.1:p.Ser649=
ENST00000551634.5:c.1853C=	ENSP00000448373.1:p.Ser618=
NM_001164749.1:c.1931C=	NP_001158221.1:p.Ser644=
NM_001165893.1:c.1841C=	NP_001159365.1:p.Ser614=
NM_022123.2:c.1835C=	NP_071406.1:p.Ser612=
NM_173159.2:c.1892C=	NP_775182.1:p.Ser631=
XM_005267991.2:c.1952C=	XP_005268048.1:p.Ser651=
XM_005267992.2:c.1946C=	XP_005268049.1:p.Ser649=
XM_005267993.2:c.1892C=	XP_005268050.1:p.Ser631=
XM_011537067.1:c.1982C=	XP_011535369.1:p.Ser661=
XM_011537068.1:c.1973C=	XP_011535370.1:p.Ser658=
XM_011537069.1:c.1943C=	XP_011535371.1:p.Ser648=
XM_011537070.1:c.1886C=	XP_011535372.1:p.Ser629=
XM_011537071.1:c.1853C=	XP_011535373.1:p.Ser618=
XM_011537072.1:c.1832C=	XP_011535374.1:p.Ser611=
XM_011537073.1:c.1625C=	XP_011535375.1:p.Ser542=
XM_011537074.1:c.1625C=	XP_011535376.1:p.Ser542=
XM_005267991.3:c.2039C=	XP_005268048.2:p.Ser680=
XM_005267992.3:c.2033C=	XP_005268049.2:p.Ser678=
XM_011537067.2:c.1982C=	XP_011535369.1:p.Ser661=
XM_011537069.2:c.2030C=	XP_011535371.2:p.Ser677=
XM_011537070.2:c.1886C=	XP_011535372.1:p.Ser629=
XM_011537071.2:c.1940C=	XP_011535373.2:p.Ser647=
XM_011537072.2:c.1832C=	XP_011535374.1:p.Ser611=
XM_017021582.1:c.2090C=	XP_016877071.1:p.Ser697=
XM_017021583.1:c.2081C=	XP_016877072.1:p.Ser694=
XM_017021584.1:c.2000C=	XP_016877073.1:p.Ser667=
XM_017021585.1:c.1949C=	XP_016877074.1:p.Ser650=
XM_017021586.1:c.1625C=	XP_016877075.1:p.Ser542=
XM_017021587.1:c.1625C=	XP_016877076.1:p.Ser542=
XM_017021588.1:c.1625C=	XP_016877077.1:p.Ser542=
NM_001164749.2:c.1931C= MANE Select	NP_001158221.1:p.Ser644=
NM_001165893.2:c.1841C=	NP_001159365.1:p.Ser614=
NM_022123.3:c.1835C=	NP_071406.1:p.Ser612=
NM_173159.3:c.1892C=	NP_775182.1:p.Ser631=
NM_001394988.1:c.1886C=	NP_001381917.1:p.Ser629=
NM_001394989.1:c.1832C=	NP_001381918.1:p.Ser611=