Canonical Allele Identifier: CA2128326746

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800038_33800056delinsCGACAGCGCCAAGGACTCG , CM000676.2:g.33800038_33800056delinsCGACAGCGCCAAGGACTCG	GRCh38
NC_000014.8:g.34269244_34269262delinsCGACAGCGCCAAGGACTCG , CM000676.1:g.34269244_34269262delinsCGACAGCGCCAAGGACTCG	GRCh37
NC_000014.7:g.33338995_33339013delinsCGACAGCGCCAAGGACTCG	NCBI36
NG_013036.1:g.865786_865804delinsCGACAGCGCCAAGGACTCG
NG_013036.2:g.865786_865804delinsCGACAGCGCCAAGGACTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1731_1749delinsCGACAGCGCCAAGGACTCG MANE Select	ENSP00000348460.4:p.Ser577=
ENST00000551634.6:c.1740_1758delinsCGACAGCGCCAAGGACTCG	ENSP00000448373.2:p.Ser580=
ENST00000680362.1:c.1631_1649delinsCGACAGCGCCAAGGACTCG
ENST00000681323.1:c.793+2457_793+2475delinsCGACAGCGCCAAGGACTCG
ENST00000346562.6:c.1635_1653delinsCGACAGCGCCAAGGACTCG	ENSP00000319610.5:p.Ser545=
ENST00000356141.8:c.1731_1749delinsCGACAGCGCCAAGGACTCG	ENSP00000348460.4:p.Ser577=
ENST00000357798.9:c.1692_1710delinsCGACAGCGCCAAGGACTCG	ENSP00000350446.5:p.Ser564=
ENST00000548645.5:c.1641_1659delinsCGACAGCGCCAAGGACTCG	ENSP00000448916.1:p.Ser547=
ENST00000551492.5:c.1746_1764delinsCGACAGCGCCAAGGACTCG	ENSP00000450392.1:p.Ser582=
ENST00000551634.5:c.1653_1671delinsCGACAGCGCCAAGGACTCG	ENSP00000448373.1:p.Ser551=
NM_001164749.1:c.1731_1749delinsCGACAGCGCCAAGGACTCG	NP_001158221.1:p.Ser577=
NM_001165893.1:c.1641_1659delinsCGACAGCGCCAAGGACTCG	NP_001159365.1:p.Ser547=
NM_022123.2:c.1635_1653delinsCGACAGCGCCAAGGACTCG	NP_071406.1:p.Ser545=
NM_173159.2:c.1692_1710delinsCGACAGCGCCAAGGACTCG	NP_775182.1:p.Ser564=
XM_005267991.2:c.1752_1770delinsCGACAGCGCCAAGGACTCG	XP_005268048.1:p.Ser584=
XM_005267992.2:c.1746_1764delinsCGACAGCGCCAAGGACTCG	XP_005268049.1:p.Ser582=
XM_005267993.2:c.1692_1710delinsCGACAGCGCCAAGGACTCG	XP_005268050.1:p.Ser564=
XM_011537067.1:c.1782_1800delinsCGACAGCGCCAAGGACTCG	XP_011535369.1:p.Ser594=
XM_011537068.1:c.1773_1791delinsCGACAGCGCCAAGGACTCG	XP_011535370.1:p.Ser591=
XM_011537069.1:c.1743_1761delinsCGACAGCGCCAAGGACTCG	XP_011535371.1:p.Ser581=
XM_011537070.1:c.1686_1704delinsCGACAGCGCCAAGGACTCG	XP_011535372.1:p.Ser562=
XM_011537071.1:c.1653_1671delinsCGACAGCGCCAAGGACTCG	XP_011535373.1:p.Ser551=
XM_011537072.1:c.1632_1650delinsCGACAGCGCCAAGGACTCG	XP_011535374.1:p.Ser544=
XM_011537073.1:c.1425_1443delinsCGACAGCGCCAAGGACTCG	XP_011535375.1:p.Ser475=
XM_011537074.1:c.1425_1443delinsCGACAGCGCCAAGGACTCG	XP_011535376.1:p.Ser475=
XM_005267991.3:c.1839_1857delinsCGACAGCGCCAAGGACTCG	XP_005268048.2:p.Ser613=
XM_005267992.3:c.1833_1851delinsCGACAGCGCCAAGGACTCG	XP_005268049.2:p.Ser611=
XM_011537067.2:c.1782_1800delinsCGACAGCGCCAAGGACTCG	XP_011535369.1:p.Ser594=
XM_011537069.2:c.1830_1848delinsCGACAGCGCCAAGGACTCG	XP_011535371.2:p.Ser610=
XM_011537070.2:c.1686_1704delinsCGACAGCGCCAAGGACTCG	XP_011535372.1:p.Ser562=
XM_011537071.2:c.1740_1758delinsCGACAGCGCCAAGGACTCG	XP_011535373.2:p.Ser580=
XM_011537072.2:c.1632_1650delinsCGACAGCGCCAAGGACTCG	XP_011535374.1:p.Ser544=
XM_017021582.1:c.1890_1908delinsCGACAGCGCCAAGGACTCG	XP_016877071.1:p.Ser630=
XM_017021583.1:c.1881_1899delinsCGACAGCGCCAAGGACTCG	XP_016877072.1:p.Ser627=
XM_017021584.1:c.1800_1818delinsCGACAGCGCCAAGGACTCG	XP_016877073.1:p.Ser600=
XM_017021585.1:c.1749_1767delinsCGACAGCGCCAAGGACTCG	XP_016877074.1:p.Ser583=
XM_017021586.1:c.1425_1443delinsCGACAGCGCCAAGGACTCG	XP_016877075.1:p.Ser475=
XM_017021587.1:c.1425_1443delinsCGACAGCGCCAAGGACTCG	XP_016877076.1:p.Ser475=
XM_017021588.1:c.1425_1443delinsCGACAGCGCCAAGGACTCG	XP_016877077.1:p.Ser475=
NM_001164749.2:c.1731_1749delinsCGACAGCGCCAAGGACTCG MANE Select	NP_001158221.1:p.Ser577=
NM_001165893.2:c.1641_1659delinsCGACAGCGCCAAGGACTCG	NP_001159365.1:p.Ser547=
NM_022123.3:c.1635_1653delinsCGACAGCGCCAAGGACTCG	NP_071406.1:p.Ser545=
NM_173159.3:c.1692_1710delinsCGACAGCGCCAAGGACTCG	NP_775182.1:p.Ser564=
NM_001394988.1:c.1686_1704delinsCGACAGCGCCAAGGACTCG	NP_001381917.1:p.Ser562=
NM_001394989.1:c.1632_1650delinsCGACAGCGCCAAGGACTCG	NP_001381918.1:p.Ser544=