Canonical Allele Identifier: CA2128327474

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800429C= , CM000676.2:g.33800429C=	GRCh38
NC_000014.8:g.34269635C= , CM000676.1:g.34269635C=	GRCh37
NC_000014.7:g.33339386C=	NCBI36
NG_013036.1:g.866177C=
NG_013036.2:g.866177C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2122C= MANE Select	ENSP00000348460.4:p.His708=
ENST00000551634.6:c.2131C=	ENSP00000448373.2:p.His711=
ENST00000680362.1:c.2022C=
ENST00000681323.1:c.793+2848C=
ENST00000346562.6:c.2026C=	ENSP00000319610.5:p.His676=
ENST00000356141.8:c.2122C=	ENSP00000348460.4:p.His708=
ENST00000357798.9:c.2083C=	ENSP00000350446.5:p.His695=
ENST00000548645.5:c.2032C=	ENSP00000448916.1:p.His678=
ENST00000551492.5:c.2137C=	ENSP00000450392.1:p.His713=
ENST00000551634.5:c.2044C=	ENSP00000448373.1:p.His682=
NM_001164749.1:c.2122C=	NP_001158221.1:p.His708=
NM_001165893.1:c.2032C=	NP_001159365.1:p.His678=
NM_022123.2:c.2026C=	NP_071406.1:p.His676=
NM_173159.2:c.2083C=	NP_775182.1:p.His695=
XM_005267991.2:c.2143C=	XP_005268048.1:p.His715=
XM_005267992.2:c.2137C=	XP_005268049.1:p.His713=
XM_005267993.2:c.2083C=	XP_005268050.1:p.His695=
XM_011537067.1:c.2173C=	XP_011535369.1:p.His725=
XM_011537068.1:c.2164C=	XP_011535370.1:p.His722=
XM_011537069.1:c.2134C=	XP_011535371.1:p.His712=
XM_011537070.1:c.2077C=	XP_011535372.1:p.His693=
XM_011537071.1:c.2044C=	XP_011535373.1:p.His682=
XM_011537072.1:c.2023C=	XP_011535374.1:p.His675=
XM_011537073.1:c.1816C=	XP_011535375.1:p.His606=
XM_011537074.1:c.1816C=	XP_011535376.1:p.His606=
XM_005267991.3:c.2230C=	XP_005268048.2:p.His744=
XM_005267992.3:c.2224C=	XP_005268049.2:p.His742=
XM_011537067.2:c.2173C=	XP_011535369.1:p.His725=
XM_011537069.2:c.2221C=	XP_011535371.2:p.His741=
XM_011537070.2:c.2077C=	XP_011535372.1:p.His693=
XM_011537071.2:c.2131C=	XP_011535373.2:p.His711=
XM_011537072.2:c.2023C=	XP_011535374.1:p.His675=
XM_017021582.1:c.2281C=	XP_016877071.1:p.His761=
XM_017021583.1:c.2272C=	XP_016877072.1:p.His758=
XM_017021584.1:c.2191C=	XP_016877073.1:p.His731=
XM_017021585.1:c.2140C=	XP_016877074.1:p.His714=
XM_017021586.1:c.1816C=	XP_016877075.1:p.His606=
XM_017021587.1:c.1816C=	XP_016877076.1:p.His606=
XM_017021588.1:c.1816C=	XP_016877077.1:p.His606=
NM_001164749.2:c.2122C= MANE Select	NP_001158221.1:p.His708=
NM_001165893.2:c.2032C=	NP_001159365.1:p.His678=
NM_022123.3:c.2026C=	NP_071406.1:p.His676=
NM_173159.3:c.2083C=	NP_775182.1:p.His695=
NM_001394988.1:c.2077C=	NP_001381917.1:p.His693=
NM_001394989.1:c.2023C=	NP_001381918.1:p.His675=