Canonical Allele Identifier: CA486093377

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269757A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800551A>T , CM000676.2:g.33800551A>T	GRCh38
NC_000014.8:g.34269757A>T , CM000676.1:g.34269757A>T	GRCh37
NC_000014.7:g.33339508A>T	NCBI36
NG_013036.1:g.866299A>T
NG_013036.2:g.866299A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2244A>T MANE Select	ENSP00000348460.4:p.Ser748=
ENST00000551634.6:c.2253A>T	ENSP00000448373.2:p.Ser751=
ENST00000680362.1:c.2144A>T
ENST00000681323.1:c.793+2970A>T
ENST00000346562.6:c.2148A>T	ENSP00000319610.5:p.Ser716=
ENST00000356141.8:c.2244A>T	ENSP00000348460.4:p.Ser748=
ENST00000357798.9:c.2205A>T	ENSP00000350446.5:p.Ser735=
ENST00000548645.5:c.2154A>T	ENSP00000448916.1:p.Ser718=
ENST00000551492.5:c.2259A>T	ENSP00000450392.1:p.Ser753=
ENST00000551634.5:c.2166A>T	ENSP00000448373.1:p.Ser722=
NM_001164749.1:c.2244A>T	NP_001158221.1:p.Ser748=
NM_001165893.1:c.2154A>T	NP_001159365.1:p.Ser718=
NM_022123.2:c.2148A>T	NP_071406.1:p.Ser716=
NM_173159.2:c.2205A>T	NP_775182.1:p.Ser735=
XM_005267991.2:c.2265A>T	XP_005268048.1:p.Ser755=
XM_005267992.2:c.2259A>T	XP_005268049.1:p.Ser753=
XM_005267993.2:c.2205A>T	XP_005268050.1:p.Ser735=
XM_011537067.1:c.2295A>T	XP_011535369.1:p.Ser765=
XM_011537068.1:c.2286A>T	XP_011535370.1:p.Ser762=
XM_011537069.1:c.2256A>T	XP_011535371.1:p.Ser752=
XM_011537070.1:c.2199A>T	XP_011535372.1:p.Ser733=
XM_011537071.1:c.2166A>T	XP_011535373.1:p.Ser722=
XM_011537072.1:c.2145A>T	XP_011535374.1:p.Ser715=
XM_011537073.1:c.1938A>T	XP_011535375.1:p.Ser646=
XM_011537074.1:c.1938A>T	XP_011535376.1:p.Ser646=
XM_005267991.3:c.2352A>T	XP_005268048.2:p.Ser784=
XM_005267992.3:c.2346A>T	XP_005268049.2:p.Ser782=
XM_011537067.2:c.2295A>T	XP_011535369.1:p.Ser765=
XM_011537069.2:c.2343A>T	XP_011535371.2:p.Ser781=
XM_011537070.2:c.2199A>T	XP_011535372.1:p.Ser733=
XM_011537071.2:c.2253A>T	XP_011535373.2:p.Ser751=
XM_011537072.2:c.2145A>T	XP_011535374.1:p.Ser715=
XM_017021582.1:c.2403A>T	XP_016877071.1:p.Ser801=
XM_017021583.1:c.2394A>T	XP_016877072.1:p.Ser798=
XM_017021584.1:c.2313A>T	XP_016877073.1:p.Ser771=
XM_017021585.1:c.2262A>T	XP_016877074.1:p.Ser754=
XM_017021586.1:c.1938A>T	XP_016877075.1:p.Ser646=
XM_017021587.1:c.1938A>T	XP_016877076.1:p.Ser646=
XM_017021588.1:c.1938A>T	XP_016877077.1:p.Ser646=
NM_001164749.2:c.2244A>T MANE Select	NP_001158221.1:p.Ser748=
NM_001165893.2:c.2154A>T	NP_001159365.1:p.Ser718=
NM_022123.3:c.2148A>T	NP_071406.1:p.Ser716=
NM_173159.3:c.2205A>T	NP_775182.1:p.Ser735=
NM_001394988.1:c.2199A>T	NP_001381917.1:p.Ser733=
NM_001394989.1:c.2145A>T	NP_001381918.1:p.Ser715=