Canonical Allele Identifier: CA2128327218

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800286_33800290delinsATGAC , CM000676.2:g.33800286_33800290delinsATGAC	GRCh38
NC_000014.8:g.34269492_34269496delinsATGAC , CM000676.1:g.34269492_34269496delinsATGAC	GRCh37
NC_000014.7:g.33339243_33339247delinsATGAC	NCBI36
NG_013036.1:g.866034_866038delinsATGAC
NG_013036.2:g.866034_866038delinsATGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1979_1983delinsATGAC MANE Select	ENSP00000348460.4:p.Asn660=
ENST00000551634.6:c.1988_1992delinsATGAC	ENSP00000448373.2:p.Asn663=
ENST00000680362.1:c.1879_1883delinsATGAC
ENST00000681323.1:c.793+2705_793+2709delinsATGAC
ENST00000346562.6:c.1883_1887delinsATGAC	ENSP00000319610.5:p.Asn628=
ENST00000356141.8:c.1979_1983delinsATGAC	ENSP00000348460.4:p.Asn660=
ENST00000357798.9:c.1940_1944delinsATGAC	ENSP00000350446.5:p.Asn647=
ENST00000548645.5:c.1889_1893delinsATGAC	ENSP00000448916.1:p.Asn630=
ENST00000551492.5:c.1994_1998delinsATGAC	ENSP00000450392.1:p.Asn665=
ENST00000551634.5:c.1901_1905delinsATGAC	ENSP00000448373.1:p.Asn634=
NM_001164749.1:c.1979_1983delinsATGAC	NP_001158221.1:p.Asn660=
NM_001165893.1:c.1889_1893delinsATGAC	NP_001159365.1:p.Asn630=
NM_022123.2:c.1883_1887delinsATGAC	NP_071406.1:p.Asn628=
NM_173159.2:c.1940_1944delinsATGAC	NP_775182.1:p.Asn647=
XM_005267991.2:c.2000_2004delinsATGAC	XP_005268048.1:p.Asn667=
XM_005267992.2:c.1994_1998delinsATGAC	XP_005268049.1:p.Asn665=
XM_005267993.2:c.1940_1944delinsATGAC	XP_005268050.1:p.Asn647=
XM_011537067.1:c.2030_2034delinsATGAC	XP_011535369.1:p.Asn677=
XM_011537068.1:c.2021_2025delinsATGAC	XP_011535370.1:p.Asn674=
XM_011537069.1:c.1991_1995delinsATGAC	XP_011535371.1:p.Asn664=
XM_011537070.1:c.1934_1938delinsATGAC	XP_011535372.1:p.Asn645=
XM_011537071.1:c.1901_1905delinsATGAC	XP_011535373.1:p.Asn634=
XM_011537072.1:c.1880_1884delinsATGAC	XP_011535374.1:p.Asn627=
XM_011537073.1:c.1673_1677delinsATGAC	XP_011535375.1:p.Asn558=
XM_011537074.1:c.1673_1677delinsATGAC	XP_011535376.1:p.Asn558=
XM_005267991.3:c.2087_2091delinsATGAC	XP_005268048.2:p.Asn696=
XM_005267992.3:c.2081_2085delinsATGAC	XP_005268049.2:p.Asn694=
XM_011537067.2:c.2030_2034delinsATGAC	XP_011535369.1:p.Asn677=
XM_011537069.2:c.2078_2082delinsATGAC	XP_011535371.2:p.Asn693=
XM_011537070.2:c.1934_1938delinsATGAC	XP_011535372.1:p.Asn645=
XM_011537071.2:c.1988_1992delinsATGAC	XP_011535373.2:p.Asn663=
XM_011537072.2:c.1880_1884delinsATGAC	XP_011535374.1:p.Asn627=
XM_017021582.1:c.2138_2142delinsATGAC	XP_016877071.1:p.Asn713=
XM_017021583.1:c.2129_2133delinsATGAC	XP_016877072.1:p.Asn710=
XM_017021584.1:c.2048_2052delinsATGAC	XP_016877073.1:p.Asn683=
XM_017021585.1:c.1997_2001delinsATGAC	XP_016877074.1:p.Asn666=
XM_017021586.1:c.1673_1677delinsATGAC	XP_016877075.1:p.Asn558=
XM_017021587.1:c.1673_1677delinsATGAC	XP_016877076.1:p.Asn558=
XM_017021588.1:c.1673_1677delinsATGAC	XP_016877077.1:p.Asn558=
NM_001164749.2:c.1979_1983delinsATGAC MANE Select	NP_001158221.1:p.Asn660=
NM_001165893.2:c.1889_1893delinsATGAC	NP_001159365.1:p.Asn630=
NM_022123.3:c.1883_1887delinsATGAC	NP_071406.1:p.Asn628=
NM_173159.3:c.1940_1944delinsATGAC	NP_775182.1:p.Asn647=
NM_001394988.1:c.1934_1938delinsATGAC	NP_001381917.1:p.Asn645=
NM_001394989.1:c.1880_1884delinsATGAC	NP_001381918.1:p.Asn627=