Canonical Allele Identifier: CA486093065

Gene: NPAS3

Linked Data

• dbSNP Id: rs1301004489
• MyVariant Identifiers: chr14:g.34269580G>A (hg19) ; chr14:g.33800374G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800374G>A , CM000676.2:g.33800374G>A	GRCh38
NC_000014.8:g.34269580G>A , CM000676.1:g.34269580G>A	GRCh37
NC_000014.7:g.33339331G>A	NCBI36
NG_013036.1:g.866122G>A
NG_013036.2:g.866122G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2067G>A MANE Select	ENSP00000348460.4:p.Glu689=
ENST00000551634.6:c.2076G>A	ENSP00000448373.2:p.Glu692=
ENST00000680362.1:c.1967G>A
ENST00000681323.1:c.793+2793G>A
ENST00000346562.6:c.1971G>A	ENSP00000319610.5:p.Glu657=
ENST00000356141.8:c.2067G>A	ENSP00000348460.4:p.Glu689=
ENST00000357798.9:c.2028G>A	ENSP00000350446.5:p.Glu676=
ENST00000548645.5:c.1977G>A	ENSP00000448916.1:p.Glu659=
ENST00000551492.5:c.2082G>A	ENSP00000450392.1:p.Glu694=
ENST00000551634.5:c.1989G>A	ENSP00000448373.1:p.Glu663=
NM_001164749.1:c.2067G>A	NP_001158221.1:p.Glu689=
NM_001165893.1:c.1977G>A	NP_001159365.1:p.Glu659=
NM_022123.2:c.1971G>A	NP_071406.1:p.Glu657=
NM_173159.2:c.2028G>A	NP_775182.1:p.Glu676=
XM_005267991.2:c.2088G>A	XP_005268048.1:p.Glu696=
XM_005267992.2:c.2082G>A	XP_005268049.1:p.Glu694=
XM_005267993.2:c.2028G>A	XP_005268050.1:p.Glu676=
XM_011537067.1:c.2118G>A	XP_011535369.1:p.Glu706=
XM_011537068.1:c.2109G>A	XP_011535370.1:p.Glu703=
XM_011537069.1:c.2079G>A	XP_011535371.1:p.Glu693=
XM_011537070.1:c.2022G>A	XP_011535372.1:p.Glu674=
XM_011537071.1:c.1989G>A	XP_011535373.1:p.Glu663=
XM_011537072.1:c.1968G>A	XP_011535374.1:p.Glu656=
XM_011537073.1:c.1761G>A	XP_011535375.1:p.Glu587=
XM_011537074.1:c.1761G>A	XP_011535376.1:p.Glu587=
XM_005267991.3:c.2175G>A	XP_005268048.2:p.Glu725=
XM_005267992.3:c.2169G>A	XP_005268049.2:p.Glu723=
XM_011537067.2:c.2118G>A	XP_011535369.1:p.Glu706=
XM_011537069.2:c.2166G>A	XP_011535371.2:p.Glu722=
XM_011537070.2:c.2022G>A	XP_011535372.1:p.Glu674=
XM_011537071.2:c.2076G>A	XP_011535373.2:p.Glu692=
XM_011537072.2:c.1968G>A	XP_011535374.1:p.Glu656=
XM_017021582.1:c.2226G>A	XP_016877071.1:p.Glu742=
XM_017021583.1:c.2217G>A	XP_016877072.1:p.Glu739=
XM_017021584.1:c.2136G>A	XP_016877073.1:p.Glu712=
XM_017021585.1:c.2085G>A	XP_016877074.1:p.Glu695=
XM_017021586.1:c.1761G>A	XP_016877075.1:p.Glu587=
XM_017021587.1:c.1761G>A	XP_016877076.1:p.Glu587=
XM_017021588.1:c.1761G>A	XP_016877077.1:p.Glu587=
NM_001164749.2:c.2067G>A MANE Select	NP_001158221.1:p.Glu689=
NM_001165893.2:c.1977G>A	NP_001159365.1:p.Glu659=
NM_022123.3:c.1971G>A	NP_071406.1:p.Glu657=
NM_173159.3:c.2028G>A	NP_775182.1:p.Glu676=
NM_001394988.1:c.2022G>A	NP_001381917.1:p.Glu674=
NM_001394989.1:c.1968G>A	NP_001381918.1:p.Glu656=