Canonical Allele Identifier: CA2832561242

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800208dup , CM000676.2:g.33800208dup	GRCh38
NC_000014.8:g.34269414dup , CM000676.1:g.34269414dup	GRCh37
NC_000014.7:g.33339165dup	NCBI36
NG_013036.1:g.865956dup
NG_013036.2:g.865956dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1901dup MANE Select	ENSP00000348460.4:p.Arg635AlafsTer27
ENST00000551634.6:c.1910dup	ENSP00000448373.2:p.Arg638AlafsTer27
ENST00000680362.1:c.1801dup
ENST00000681323.1:c.793+2627dup
ENST00000346562.6:c.1805dup	ENSP00000319610.5:p.Arg603AlafsTer27
ENST00000356141.8:c.1901dup	ENSP00000348460.4:p.Arg635AlafsTer27
ENST00000357798.9:c.1862dup	ENSP00000350446.5:p.Arg622AlafsTer27
ENST00000548645.5:c.1811dup	ENSP00000448916.1:p.Arg605AlafsTer27
ENST00000551492.5:c.1916dup	ENSP00000450392.1:p.Arg640AlafsTer27
ENST00000551634.5:c.1823dup	ENSP00000448373.1:p.Arg609AlafsTer27
NM_001164749.1:c.1901dup	NP_001158221.1:p.Arg635AlafsTer27
NM_001165893.1:c.1811dup	NP_001159365.1:p.Arg605AlafsTer27
NM_022123.2:c.1805dup	NP_071406.1:p.Arg603AlafsTer27
NM_173159.2:c.1862dup	NP_775182.1:p.Arg622AlafsTer27
XM_005267991.2:c.1922dup	XP_005268048.1:p.Arg642AlafsTer27
XM_005267992.2:c.1916dup	XP_005268049.1:p.Arg640AlafsTer27
XM_005267993.2:c.1862dup	XP_005268050.1:p.Arg622AlafsTer27
XM_011537067.1:c.1952dup	XP_011535369.1:p.Arg652AlafsTer27
XM_011537068.1:c.1943dup	XP_011535370.1:p.Arg649AlafsTer27
XM_011537069.1:c.1913dup	XP_011535371.1:p.Arg639AlafsTer27
XM_011537070.1:c.1856dup	XP_011535372.1:p.Arg620AlafsTer27
XM_011537071.1:c.1823dup	XP_011535373.1:p.Arg609AlafsTer27
XM_011537072.1:c.1802dup	XP_011535374.1:p.Arg602AlafsTer27
XM_011537073.1:c.1595dup	XP_011535375.1:p.Arg533AlafsTer27
XM_011537074.1:c.1595dup	XP_011535376.1:p.Arg533AlafsTer27
XM_005267991.3:c.2009dup	XP_005268048.2:p.Arg671AlafsTer27
XM_005267992.3:c.2003dup	XP_005268049.2:p.Arg669AlafsTer27
XM_011537067.2:c.1952dup	XP_011535369.1:p.Arg652AlafsTer27
XM_011537069.2:c.2000dup	XP_011535371.2:p.Arg668AlafsTer27
XM_011537070.2:c.1856dup	XP_011535372.1:p.Arg620AlafsTer27
XM_011537071.2:c.1910dup	XP_011535373.2:p.Arg638AlafsTer27
XM_011537072.2:c.1802dup	XP_011535374.1:p.Arg602AlafsTer27
XM_017021582.1:c.2060dup	XP_016877071.1:p.Arg688AlafsTer27
XM_017021583.1:c.2051dup	XP_016877072.1:p.Arg685AlafsTer27
XM_017021584.1:c.1970dup	XP_016877073.1:p.Arg658AlafsTer27
XM_017021585.1:c.1919dup	XP_016877074.1:p.Arg641AlafsTer27
XM_017021586.1:c.1595dup	XP_016877075.1:p.Arg533AlafsTer27
XM_017021587.1:c.1595dup	XP_016877076.1:p.Arg533AlafsTer27
XM_017021588.1:c.1595dup	XP_016877077.1:p.Arg533AlafsTer27
NM_001164749.2:c.1901dup MANE Select	NP_001158221.1:p.Arg635AlafsTer27
NM_001165893.2:c.1811dup	NP_001159365.1:p.Arg605AlafsTer27
NM_022123.3:c.1805dup	NP_071406.1:p.Arg603AlafsTer27
NM_173159.3:c.1862dup	NP_775182.1:p.Arg622AlafsTer27
NM_001394988.1:c.1856dup	NP_001381917.1:p.Arg620AlafsTer27
NM_001394989.1:c.1802dup	NP_001381918.1:p.Arg602AlafsTer27