Canonical Allele Identifier: CA2128326879

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800110_33800111delinsGA , CM000676.2:g.33800110_33800111delinsGA	GRCh38
NC_000014.8:g.34269316_34269317delinsGA , CM000676.1:g.34269316_34269317delinsGA	GRCh37
NC_000014.7:g.33339067_33339068delinsGA	NCBI36
NG_013036.1:g.865858_865859delinsGA
NG_013036.2:g.865858_865859delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1803_1804delinsGA MANE Select	ENSP00000348460.4:p.Lys601=
ENST00000551634.6:c.1812_1813delinsGA	ENSP00000448373.2:p.Lys604=
ENST00000680362.1:c.1703_1704delinsGA
ENST00000681323.1:c.793+2529_793+2530delinsGA
ENST00000346562.6:c.1707_1708delinsGA	ENSP00000319610.5:p.Lys569=
ENST00000356141.8:c.1803_1804delinsGA	ENSP00000348460.4:p.Lys601=
ENST00000357798.9:c.1764_1765delinsGA	ENSP00000350446.5:p.Lys588=
ENST00000548645.5:c.1713_1714delinsGA	ENSP00000448916.1:p.Lys571=
ENST00000551492.5:c.1818_1819delinsGA	ENSP00000450392.1:p.Lys606=
ENST00000551634.5:c.1725_1726delinsGA	ENSP00000448373.1:p.Lys575=
NM_001164749.1:c.1803_1804delinsGA	NP_001158221.1:p.Lys601=
NM_001165893.1:c.1713_1714delinsGA	NP_001159365.1:p.Lys571=
NM_022123.2:c.1707_1708delinsGA	NP_071406.1:p.Lys569=
NM_173159.2:c.1764_1765delinsGA	NP_775182.1:p.Lys588=
XM_005267991.2:c.1824_1825delinsGA	XP_005268048.1:p.Lys608=
XM_005267992.2:c.1818_1819delinsGA	XP_005268049.1:p.Lys606=
XM_005267993.2:c.1764_1765delinsGA	XP_005268050.1:p.Lys588=
XM_011537067.1:c.1854_1855delinsGA	XP_011535369.1:p.Lys618=
XM_011537068.1:c.1845_1846delinsGA	XP_011535370.1:p.Lys615=
XM_011537069.1:c.1815_1816delinsGA	XP_011535371.1:p.Lys605=
XM_011537070.1:c.1758_1759delinsGA	XP_011535372.1:p.Lys586=
XM_011537071.1:c.1725_1726delinsGA	XP_011535373.1:p.Lys575=
XM_011537072.1:c.1704_1705delinsGA	XP_011535374.1:p.Lys568=
XM_011537073.1:c.1497_1498delinsGA	XP_011535375.1:p.Lys499=
XM_011537074.1:c.1497_1498delinsGA	XP_011535376.1:p.Lys499=
XM_005267991.3:c.1911_1912delinsGA	XP_005268048.2:p.Lys637=
XM_005267992.3:c.1905_1906delinsGA	XP_005268049.2:p.Lys635=
XM_011537067.2:c.1854_1855delinsGA	XP_011535369.1:p.Lys618=
XM_011537069.2:c.1902_1903delinsGA	XP_011535371.2:p.Lys634=
XM_011537070.2:c.1758_1759delinsGA	XP_011535372.1:p.Lys586=
XM_011537071.2:c.1812_1813delinsGA	XP_011535373.2:p.Lys604=
XM_011537072.2:c.1704_1705delinsGA	XP_011535374.1:p.Lys568=
XM_017021582.1:c.1962_1963delinsGA	XP_016877071.1:p.Lys654=
XM_017021583.1:c.1953_1954delinsGA	XP_016877072.1:p.Lys651=
XM_017021584.1:c.1872_1873delinsGA	XP_016877073.1:p.Lys624=
XM_017021585.1:c.1821_1822delinsGA	XP_016877074.1:p.Lys607=
XM_017021586.1:c.1497_1498delinsGA	XP_016877075.1:p.Lys499=
XM_017021587.1:c.1497_1498delinsGA	XP_016877076.1:p.Lys499=
XM_017021588.1:c.1497_1498delinsGA	XP_016877077.1:p.Lys499=
NM_001164749.2:c.1803_1804delinsGA MANE Select	NP_001158221.1:p.Lys601=
NM_001165893.2:c.1713_1714delinsGA	NP_001159365.1:p.Lys571=
NM_022123.3:c.1707_1708delinsGA	NP_071406.1:p.Lys569=
NM_173159.3:c.1764_1765delinsGA	NP_775182.1:p.Lys588=
NM_001394988.1:c.1758_1759delinsGA	NP_001381917.1:p.Lys586=
NM_001394989.1:c.1704_1705delinsGA	NP_001381918.1:p.Lys568=