Canonical Allele Identifier: CA2128327268

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800332G= , CM000676.2:g.33800332G=	GRCh38
NC_000014.8:g.34269538G= , CM000676.1:g.34269538G=	GRCh37
NC_000014.7:g.33339289G=	NCBI36
NG_013036.1:g.866080G=
NG_013036.2:g.866080G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2025G= MANE Select	ENSP00000348460.4:p.Arg675=
ENST00000551634.6:c.2034G=	ENSP00000448373.2:p.Arg678=
ENST00000680362.1:c.1925G=
ENST00000681323.1:c.793+2751G=
ENST00000346562.6:c.1929G=	ENSP00000319610.5:p.Arg643=
ENST00000356141.8:c.2025G=	ENSP00000348460.4:p.Arg675=
ENST00000357798.9:c.1986G=	ENSP00000350446.5:p.Arg662=
ENST00000548645.5:c.1935G=	ENSP00000448916.1:p.Arg645=
ENST00000551492.5:c.2040G=	ENSP00000450392.1:p.Arg680=
ENST00000551634.5:c.1947G=	ENSP00000448373.1:p.Arg649=
NM_001164749.1:c.2025G=	NP_001158221.1:p.Arg675=
NM_001165893.1:c.1935G=	NP_001159365.1:p.Arg645=
NM_022123.2:c.1929G=	NP_071406.1:p.Arg643=
NM_173159.2:c.1986G=	NP_775182.1:p.Arg662=
XM_005267991.2:c.2046G=	XP_005268048.1:p.Arg682=
XM_005267992.2:c.2040G=	XP_005268049.1:p.Arg680=
XM_005267993.2:c.1986G=	XP_005268050.1:p.Arg662=
XM_011537067.1:c.2076G=	XP_011535369.1:p.Arg692=
XM_011537068.1:c.2067G=	XP_011535370.1:p.Arg689=
XM_011537069.1:c.2037G=	XP_011535371.1:p.Arg679=
XM_011537070.1:c.1980G=	XP_011535372.1:p.Arg660=
XM_011537071.1:c.1947G=	XP_011535373.1:p.Arg649=
XM_011537072.1:c.1926G=	XP_011535374.1:p.Arg642=
XM_011537073.1:c.1719G=	XP_011535375.1:p.Arg573=
XM_011537074.1:c.1719G=	XP_011535376.1:p.Arg573=
XM_005267991.3:c.2133G=	XP_005268048.2:p.Arg711=
XM_005267992.3:c.2127G=	XP_005268049.2:p.Arg709=
XM_011537067.2:c.2076G=	XP_011535369.1:p.Arg692=
XM_011537069.2:c.2124G=	XP_011535371.2:p.Arg708=
XM_011537070.2:c.1980G=	XP_011535372.1:p.Arg660=
XM_011537071.2:c.2034G=	XP_011535373.2:p.Arg678=
XM_011537072.2:c.1926G=	XP_011535374.1:p.Arg642=
XM_017021582.1:c.2184G=	XP_016877071.1:p.Arg728=
XM_017021583.1:c.2175G=	XP_016877072.1:p.Arg725=
XM_017021584.1:c.2094G=	XP_016877073.1:p.Arg698=
XM_017021585.1:c.2043G=	XP_016877074.1:p.Arg681=
XM_017021586.1:c.1719G=	XP_016877075.1:p.Arg573=
XM_017021587.1:c.1719G=	XP_016877076.1:p.Arg573=
XM_017021588.1:c.1719G=	XP_016877077.1:p.Arg573=
NM_001164749.2:c.2025G= MANE Select	NP_001158221.1:p.Arg675=
NM_001165893.2:c.1935G=	NP_001159365.1:p.Arg645=
NM_022123.3:c.1929G=	NP_071406.1:p.Arg643=
NM_173159.3:c.1986G=	NP_775182.1:p.Arg662=
NM_001394988.1:c.1980G=	NP_001381917.1:p.Arg660=
NM_001394989.1:c.1926G=	NP_001381918.1:p.Arg642=