Canonical Allele Identifier: CA2128327146

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800240G= , CM000676.2:g.33800240G=	GRCh38
NC_000014.8:g.34269446G= , CM000676.1:g.34269446G=	GRCh37
NC_000014.7:g.33339197G=	NCBI36
NG_013036.1:g.865988G=
NG_013036.2:g.865988G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1933G= MANE Select	ENSP00000348460.4:p.Val645=
ENST00000551634.6:c.1942G=	ENSP00000448373.2:p.Val648=
ENST00000680362.1:c.1833G=
ENST00000681323.1:c.793+2659G=
ENST00000346562.6:c.1837G=	ENSP00000319610.5:p.Val613=
ENST00000356141.8:c.1933G=	ENSP00000348460.4:p.Val645=
ENST00000357798.9:c.1894G=	ENSP00000350446.5:p.Val632=
ENST00000548645.5:c.1843G=	ENSP00000448916.1:p.Val615=
ENST00000551492.5:c.1948G=	ENSP00000450392.1:p.Val650=
ENST00000551634.5:c.1855G=	ENSP00000448373.1:p.Val619=
NM_001164749.1:c.1933G=	NP_001158221.1:p.Val645=
NM_001165893.1:c.1843G=	NP_001159365.1:p.Val615=
NM_022123.2:c.1837G=	NP_071406.1:p.Val613=
NM_173159.2:c.1894G=	NP_775182.1:p.Val632=
XM_005267991.2:c.1954G=	XP_005268048.1:p.Val652=
XM_005267992.2:c.1948G=	XP_005268049.1:p.Val650=
XM_005267993.2:c.1894G=	XP_005268050.1:p.Val632=
XM_011537067.1:c.1984G=	XP_011535369.1:p.Val662=
XM_011537068.1:c.1975G=	XP_011535370.1:p.Val659=
XM_011537069.1:c.1945G=	XP_011535371.1:p.Val649=
XM_011537070.1:c.1888G=	XP_011535372.1:p.Val630=
XM_011537071.1:c.1855G=	XP_011535373.1:p.Val619=
XM_011537072.1:c.1834G=	XP_011535374.1:p.Val612=
XM_011537073.1:c.1627G=	XP_011535375.1:p.Val543=
XM_011537074.1:c.1627G=	XP_011535376.1:p.Val543=
XM_005267991.3:c.2041G=	XP_005268048.2:p.Val681=
XM_005267992.3:c.2035G=	XP_005268049.2:p.Val679=
XM_011537067.2:c.1984G=	XP_011535369.1:p.Val662=
XM_011537069.2:c.2032G=	XP_011535371.2:p.Val678=
XM_011537070.2:c.1888G=	XP_011535372.1:p.Val630=
XM_011537071.2:c.1942G=	XP_011535373.2:p.Val648=
XM_011537072.2:c.1834G=	XP_011535374.1:p.Val612=
XM_017021582.1:c.2092G=	XP_016877071.1:p.Val698=
XM_017021583.1:c.2083G=	XP_016877072.1:p.Val695=
XM_017021584.1:c.2002G=	XP_016877073.1:p.Val668=
XM_017021585.1:c.1951G=	XP_016877074.1:p.Val651=
XM_017021586.1:c.1627G=	XP_016877075.1:p.Val543=
XM_017021587.1:c.1627G=	XP_016877076.1:p.Val543=
XM_017021588.1:c.1627G=	XP_016877077.1:p.Val543=
NM_001164749.2:c.1933G= MANE Select	NP_001158221.1:p.Val645=
NM_001165893.2:c.1843G=	NP_001159365.1:p.Val615=
NM_022123.3:c.1837G=	NP_071406.1:p.Val613=
NM_173159.3:c.1894G=	NP_775182.1:p.Val632=
NM_001394988.1:c.1888G=	NP_001381917.1:p.Val630=
NM_001394989.1:c.1834G=	NP_001381918.1:p.Val612=