Canonical Allele Identifier: CA2128327072

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800207C= , CM000676.2:g.33800207C=	GRCh38
NC_000014.8:g.34269413C= , CM000676.1:g.34269413C=	GRCh37
NC_000014.7:g.33339164C=	NCBI36
NG_013036.1:g.865955C=
NG_013036.2:g.865955C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1900C= MANE Select	ENSP00000348460.4:p.Pro634=
ENST00000551634.6:c.1909C=	ENSP00000448373.2:p.Pro637=
ENST00000680362.1:c.1800C=
ENST00000681323.1:c.793+2626C=
ENST00000346562.6:c.1804C=	ENSP00000319610.5:p.Pro602=
ENST00000356141.8:c.1900C=	ENSP00000348460.4:p.Pro634=
ENST00000357798.9:c.1861C=	ENSP00000350446.5:p.Pro621=
ENST00000548645.5:c.1810C=	ENSP00000448916.1:p.Pro604=
ENST00000551492.5:c.1915C=	ENSP00000450392.1:p.Pro639=
ENST00000551634.5:c.1822C=	ENSP00000448373.1:p.Pro608=
NM_001164749.1:c.1900C=	NP_001158221.1:p.Pro634=
NM_001165893.1:c.1810C=	NP_001159365.1:p.Pro604=
NM_022123.2:c.1804C=	NP_071406.1:p.Pro602=
NM_173159.2:c.1861C=	NP_775182.1:p.Pro621=
XM_005267991.2:c.1921C=	XP_005268048.1:p.Pro641=
XM_005267992.2:c.1915C=	XP_005268049.1:p.Pro639=
XM_005267993.2:c.1861C=	XP_005268050.1:p.Pro621=
XM_011537067.1:c.1951C=	XP_011535369.1:p.Pro651=
XM_011537068.1:c.1942C=	XP_011535370.1:p.Pro648=
XM_011537069.1:c.1912C=	XP_011535371.1:p.Pro638=
XM_011537070.1:c.1855C=	XP_011535372.1:p.Pro619=
XM_011537071.1:c.1822C=	XP_011535373.1:p.Pro608=
XM_011537072.1:c.1801C=	XP_011535374.1:p.Pro601=
XM_011537073.1:c.1594C=	XP_011535375.1:p.Pro532=
XM_011537074.1:c.1594C=	XP_011535376.1:p.Pro532=
XM_005267991.3:c.2008C=	XP_005268048.2:p.Pro670=
XM_005267992.3:c.2002C=	XP_005268049.2:p.Pro668=
XM_011537067.2:c.1951C=	XP_011535369.1:p.Pro651=
XM_011537069.2:c.1999C=	XP_011535371.2:p.Pro667=
XM_011537070.2:c.1855C=	XP_011535372.1:p.Pro619=
XM_011537071.2:c.1909C=	XP_011535373.2:p.Pro637=
XM_011537072.2:c.1801C=	XP_011535374.1:p.Pro601=
XM_017021582.1:c.2059C=	XP_016877071.1:p.Pro687=
XM_017021583.1:c.2050C=	XP_016877072.1:p.Pro684=
XM_017021584.1:c.1969C=	XP_016877073.1:p.Pro657=
XM_017021585.1:c.1918C=	XP_016877074.1:p.Pro640=
XM_017021586.1:c.1594C=	XP_016877075.1:p.Pro532=
XM_017021587.1:c.1594C=	XP_016877076.1:p.Pro532=
XM_017021588.1:c.1594C=	XP_016877077.1:p.Pro532=
NM_001164749.2:c.1900C= MANE Select	NP_001158221.1:p.Pro634=
NM_001165893.2:c.1810C=	NP_001159365.1:p.Pro604=
NM_022123.3:c.1804C=	NP_071406.1:p.Pro602=
NM_173159.3:c.1861C=	NP_775182.1:p.Pro621=
NM_001394988.1:c.1855C=	NP_001381917.1:p.Pro619=
NM_001394989.1:c.1801C=	NP_001381918.1:p.Pro601=