Canonical Allele Identifier: CA2801126434

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800085_33800086insTTGGTT , CM000676.2:g.33800085_33800086insTTGGTT	GRCh38
NC_000014.8:g.34269291_34269292insTTGGTT , CM000676.1:g.34269291_34269292insTTGGTT	GRCh37
NC_000014.7:g.33339042_33339043insTTGGTT	NCBI36
NG_013036.1:g.865833_865834insTTGGTT
NG_013036.2:g.865833_865834insTTGGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1778_1779insTTGGTT MANE Select	ENSP00000348460.4:p.Ala593_Ser594insTrpPhe
ENST00000551634.6:c.1787_1788insTTGGTT	ENSP00000448373.2:p.Ala596_Ser597insTrpPhe
ENST00000680362.1:c.1678_1679insTTGGTT
ENST00000681323.1:c.793+2504_793+2505insTTGGTT
ENST00000346562.6:c.1682_1683insTTGGTT	ENSP00000319610.5:p.Ala561_Ser562insTrpPhe
ENST00000356141.8:c.1778_1779insTTGGTT	ENSP00000348460.4:p.Ala593_Ser594insTrpPhe
ENST00000357798.9:c.1739_1740insTTGGTT	ENSP00000350446.5:p.Ala580_Ser581insTrpPhe
ENST00000548645.5:c.1688_1689insTTGGTT	ENSP00000448916.1:p.Ala563_Ser564insTrpPhe
ENST00000551492.5:c.1793_1794insTTGGTT	ENSP00000450392.1:p.Ala598_Ser599insTrpPhe
ENST00000551634.5:c.1700_1701insTTGGTT	ENSP00000448373.1:p.Ala567_Ser568insTrpPhe
NM_001164749.1:c.1778_1779insTTGGTT	NP_001158221.1:p.Ala593_Ser594insTrpPhe
NM_001165893.1:c.1688_1689insTTGGTT	NP_001159365.1:p.Ala563_Ser564insTrpPhe
NM_022123.2:c.1682_1683insTTGGTT	NP_071406.1:p.Ala561_Ser562insTrpPhe
NM_173159.2:c.1739_1740insTTGGTT	NP_775182.1:p.Ala580_Ser581insTrpPhe
XM_005267991.2:c.1799_1800insTTGGTT	XP_005268048.1:p.Ala600_Ser601insTrpPhe
XM_005267992.2:c.1793_1794insTTGGTT	XP_005268049.1:p.Ala598_Ser599insTrpPhe
XM_005267993.2:c.1739_1740insTTGGTT	XP_005268050.1:p.Ala580_Ser581insTrpPhe
XM_011537067.1:c.1829_1830insTTGGTT	XP_011535369.1:p.Ala610_Ser611insTrpPhe
XM_011537068.1:c.1820_1821insTTGGTT	XP_011535370.1:p.Ala607_Ser608insTrpPhe
XM_011537069.1:c.1790_1791insTTGGTT	XP_011535371.1:p.Ala597_Ser598insTrpPhe
XM_011537070.1:c.1733_1734insTTGGTT	XP_011535372.1:p.Ala578_Ser579insTrpPhe
XM_011537071.1:c.1700_1701insTTGGTT	XP_011535373.1:p.Ala567_Ser568insTrpPhe
XM_011537072.1:c.1679_1680insTTGGTT	XP_011535374.1:p.Ala560_Ser561insTrpPhe
XM_011537073.1:c.1472_1473insTTGGTT	XP_011535375.1:p.Ala491_Ser492insTrpPhe
XM_011537074.1:c.1472_1473insTTGGTT	XP_011535376.1:p.Ala491_Ser492insTrpPhe
XM_005267991.3:c.1886_1887insTTGGTT	XP_005268048.2:p.Ala629_Ser630insTrpPhe
XM_005267992.3:c.1880_1881insTTGGTT	XP_005268049.2:p.Ala627_Ser628insTrpPhe
XM_011537067.2:c.1829_1830insTTGGTT	XP_011535369.1:p.Ala610_Ser611insTrpPhe
XM_011537069.2:c.1877_1878insTTGGTT	XP_011535371.2:p.Ala626_Ser627insTrpPhe
XM_011537070.2:c.1733_1734insTTGGTT	XP_011535372.1:p.Ala578_Ser579insTrpPhe
XM_011537071.2:c.1787_1788insTTGGTT	XP_011535373.2:p.Ala596_Ser597insTrpPhe
XM_011537072.2:c.1679_1680insTTGGTT	XP_011535374.1:p.Ala560_Ser561insTrpPhe
XM_017021582.1:c.1937_1938insTTGGTT	XP_016877071.1:p.Ala646_Ser647insTrpPhe
XM_017021583.1:c.1928_1929insTTGGTT	XP_016877072.1:p.Ala643_Ser644insTrpPhe
XM_017021584.1:c.1847_1848insTTGGTT	XP_016877073.1:p.Ala616_Ser617insTrpPhe
XM_017021585.1:c.1796_1797insTTGGTT	XP_016877074.1:p.Ala599_Ser600insTrpPhe
XM_017021586.1:c.1472_1473insTTGGTT	XP_016877075.1:p.Ala491_Ser492insTrpPhe
XM_017021587.1:c.1472_1473insTTGGTT	XP_016877076.1:p.Ala491_Ser492insTrpPhe
XM_017021588.1:c.1472_1473insTTGGTT	XP_016877077.1:p.Ala491_Ser492insTrpPhe
NM_001164749.2:c.1778_1779insTTGGTT MANE Select	NP_001158221.1:p.Ala593_Ser594insTrpPhe
NM_001165893.2:c.1688_1689insTTGGTT	NP_001159365.1:p.Ala563_Ser564insTrpPhe
NM_022123.3:c.1682_1683insTTGGTT	NP_071406.1:p.Ala561_Ser562insTrpPhe
NM_173159.3:c.1739_1740insTTGGTT	NP_775182.1:p.Ala580_Ser581insTrpPhe
NM_001394988.1:c.1733_1734insTTGGTT	NP_001381917.1:p.Ala578_Ser579insTrpPhe
NM_001394989.1:c.1679_1680insTTGGTT	NP_001381918.1:p.Ala560_Ser561insTrpPhe