Canonical Allele Identifier: CA389413525

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269528A>T (hg19) ; chr14:g.33800322A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800322A>T , CM000676.2:g.33800322A>T	GRCh38
NC_000014.8:g.34269528A>T , CM000676.1:g.34269528A>T	GRCh37
NC_000014.7:g.33339279A>T	NCBI36
NG_013036.1:g.866070A>T
NG_013036.2:g.866070A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2015A>T MANE Select	ENSP00000348460.4:p.Glu672Val
ENST00000551634.6:c.2024A>T	ENSP00000448373.2:p.Glu675Val
ENST00000680362.1:c.1915A>T
ENST00000681323.1:c.793+2741A>T
ENST00000346562.6:c.1919A>T	ENSP00000319610.5:p.Glu640Val
ENST00000356141.8:c.2015A>T	ENSP00000348460.4:p.Glu672Val
ENST00000357798.9:c.1976A>T	ENSP00000350446.5:p.Glu659Val
ENST00000548645.5:c.1925A>T	ENSP00000448916.1:p.Glu642Val
ENST00000551492.5:c.2030A>T	ENSP00000450392.1:p.Glu677Val
ENST00000551634.5:c.1937A>T	ENSP00000448373.1:p.Glu646Val
NM_001164749.1:c.2015A>T	NP_001158221.1:p.Glu672Val
NM_001165893.1:c.1925A>T	NP_001159365.1:p.Glu642Val
NM_022123.2:c.1919A>T	NP_071406.1:p.Glu640Val
NM_173159.2:c.1976A>T	NP_775182.1:p.Glu659Val
XM_005267991.2:c.2036A>T	XP_005268048.1:p.Glu679Val
XM_005267992.2:c.2030A>T	XP_005268049.1:p.Glu677Val
XM_005267993.2:c.1976A>T	XP_005268050.1:p.Glu659Val
XM_011537067.1:c.2066A>T	XP_011535369.1:p.Glu689Val
XM_011537068.1:c.2057A>T	XP_011535370.1:p.Glu686Val
XM_011537069.1:c.2027A>T	XP_011535371.1:p.Glu676Val
XM_011537070.1:c.1970A>T	XP_011535372.1:p.Glu657Val
XM_011537071.1:c.1937A>T	XP_011535373.1:p.Glu646Val
XM_011537072.1:c.1916A>T	XP_011535374.1:p.Glu639Val
XM_011537073.1:c.1709A>T	XP_011535375.1:p.Glu570Val
XM_011537074.1:c.1709A>T	XP_011535376.1:p.Glu570Val
XM_005267991.3:c.2123A>T	XP_005268048.2:p.Glu708Val
XM_005267992.3:c.2117A>T	XP_005268049.2:p.Glu706Val
XM_011537067.2:c.2066A>T	XP_011535369.1:p.Glu689Val
XM_011537069.2:c.2114A>T	XP_011535371.2:p.Glu705Val
XM_011537070.2:c.1970A>T	XP_011535372.1:p.Glu657Val
XM_011537071.2:c.2024A>T	XP_011535373.2:p.Glu675Val
XM_011537072.2:c.1916A>T	XP_011535374.1:p.Glu639Val
XM_017021582.1:c.2174A>T	XP_016877071.1:p.Glu725Val
XM_017021583.1:c.2165A>T	XP_016877072.1:p.Glu722Val
XM_017021584.1:c.2084A>T	XP_016877073.1:p.Glu695Val
XM_017021585.1:c.2033A>T	XP_016877074.1:p.Glu678Val
XM_017021586.1:c.1709A>T	XP_016877075.1:p.Glu570Val
XM_017021587.1:c.1709A>T	XP_016877076.1:p.Glu570Val
XM_017021588.1:c.1709A>T	XP_016877077.1:p.Glu570Val
NM_001164749.2:c.2015A>T MANE Select	NP_001158221.1:p.Glu672Val
NM_001165893.2:c.1925A>T	NP_001159365.1:p.Glu642Val
NM_022123.3:c.1919A>T	NP_071406.1:p.Glu640Val
NM_173159.3:c.1976A>T	NP_775182.1:p.Glu659Val
NM_001394988.1:c.1970A>T	NP_001381917.1:p.Glu657Val
NM_001394989.1:c.1916A>T	NP_001381918.1:p.Glu639Val