Canonical Allele Identifier: CA2128326820

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800073C= , CM000676.2:g.33800073C=	GRCh38
NC_000014.8:g.34269279C= , CM000676.1:g.34269279C=	GRCh37
NC_000014.7:g.33339030C=	NCBI36
NG_013036.1:g.865821C=
NG_013036.2:g.865821C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1766C= MANE Select	ENSP00000348460.4:p.Ala589=
ENST00000551634.6:c.1775C=	ENSP00000448373.2:p.Ala592=
ENST00000680362.1:c.1666C=
ENST00000681323.1:c.793+2492C=
ENST00000346562.6:c.1670C=	ENSP00000319610.5:p.Ala557=
ENST00000356141.8:c.1766C=	ENSP00000348460.4:p.Ala589=
ENST00000357798.9:c.1727C=	ENSP00000350446.5:p.Ala576=
ENST00000548645.5:c.1676C=	ENSP00000448916.1:p.Ala559=
ENST00000551492.5:c.1781C=	ENSP00000450392.1:p.Ala594=
ENST00000551634.5:c.1688C=	ENSP00000448373.1:p.Ala563=
NM_001164749.1:c.1766C=	NP_001158221.1:p.Ala589=
NM_001165893.1:c.1676C=	NP_001159365.1:p.Ala559=
NM_022123.2:c.1670C=	NP_071406.1:p.Ala557=
NM_173159.2:c.1727C=	NP_775182.1:p.Ala576=
XM_005267991.2:c.1787C=	XP_005268048.1:p.Ala596=
XM_005267992.2:c.1781C=	XP_005268049.1:p.Ala594=
XM_005267993.2:c.1727C=	XP_005268050.1:p.Ala576=
XM_011537067.1:c.1817C=	XP_011535369.1:p.Ala606=
XM_011537068.1:c.1808C=	XP_011535370.1:p.Ala603=
XM_011537069.1:c.1778C=	XP_011535371.1:p.Ala593=
XM_011537070.1:c.1721C=	XP_011535372.1:p.Ala574=
XM_011537071.1:c.1688C=	XP_011535373.1:p.Ala563=
XM_011537072.1:c.1667C=	XP_011535374.1:p.Ala556=
XM_011537073.1:c.1460C=	XP_011535375.1:p.Ala487=
XM_011537074.1:c.1460C=	XP_011535376.1:p.Ala487=
XM_005267991.3:c.1874C=	XP_005268048.2:p.Ala625=
XM_005267992.3:c.1868C=	XP_005268049.2:p.Ala623=
XM_011537067.2:c.1817C=	XP_011535369.1:p.Ala606=
XM_011537069.2:c.1865C=	XP_011535371.2:p.Ala622=
XM_011537070.2:c.1721C=	XP_011535372.1:p.Ala574=
XM_011537071.2:c.1775C=	XP_011535373.2:p.Ala592=
XM_011537072.2:c.1667C=	XP_011535374.1:p.Ala556=
XM_017021582.1:c.1925C=	XP_016877071.1:p.Ala642=
XM_017021583.1:c.1916C=	XP_016877072.1:p.Ala639=
XM_017021584.1:c.1835C=	XP_016877073.1:p.Ala612=
XM_017021585.1:c.1784C=	XP_016877074.1:p.Ala595=
XM_017021586.1:c.1460C=	XP_016877075.1:p.Ala487=
XM_017021587.1:c.1460C=	XP_016877076.1:p.Ala487=
XM_017021588.1:c.1460C=	XP_016877077.1:p.Ala487=
NM_001164749.2:c.1766C= MANE Select	NP_001158221.1:p.Ala589=
NM_001165893.2:c.1676C=	NP_001159365.1:p.Ala559=
NM_022123.3:c.1670C=	NP_071406.1:p.Ala557=
NM_173159.3:c.1727C=	NP_775182.1:p.Ala576=
NM_001394988.1:c.1721C=	NP_001381917.1:p.Ala574=
NM_001394989.1:c.1667C=	NP_001381918.1:p.Ala556=