Canonical Allele Identifier: CA389412333

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269288A>G (hg19) ; chr14:g.33800082A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800082A>G , CM000676.2:g.33800082A>G	GRCh38
NC_000014.8:g.34269288A>G , CM000676.1:g.34269288A>G	GRCh37
NC_000014.7:g.33339039A>G	NCBI36
NG_013036.1:g.865830A>G
NG_013036.2:g.865830A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1775A>G MANE Select	ENSP00000348460.4:p.Gln592Arg
ENST00000551634.6:c.1784A>G	ENSP00000448373.2:p.Gln595Arg
ENST00000680362.1:c.1675A>G
ENST00000681323.1:c.793+2501A>G
ENST00000346562.6:c.1679A>G	ENSP00000319610.5:p.Gln560Arg
ENST00000356141.8:c.1775A>G	ENSP00000348460.4:p.Gln592Arg
ENST00000357798.9:c.1736A>G	ENSP00000350446.5:p.Gln579Arg
ENST00000548645.5:c.1685A>G	ENSP00000448916.1:p.Gln562Arg
ENST00000551492.5:c.1790A>G	ENSP00000450392.1:p.Gln597Arg
ENST00000551634.5:c.1697A>G	ENSP00000448373.1:p.Gln566Arg
NM_001164749.1:c.1775A>G	NP_001158221.1:p.Gln592Arg
NM_001165893.1:c.1685A>G	NP_001159365.1:p.Gln562Arg
NM_022123.2:c.1679A>G	NP_071406.1:p.Gln560Arg
NM_173159.2:c.1736A>G	NP_775182.1:p.Gln579Arg
XM_005267991.2:c.1796A>G	XP_005268048.1:p.Gln599Arg
XM_005267992.2:c.1790A>G	XP_005268049.1:p.Gln597Arg
XM_005267993.2:c.1736A>G	XP_005268050.1:p.Gln579Arg
XM_011537067.1:c.1826A>G	XP_011535369.1:p.Gln609Arg
XM_011537068.1:c.1817A>G	XP_011535370.1:p.Gln606Arg
XM_011537069.1:c.1787A>G	XP_011535371.1:p.Gln596Arg
XM_011537070.1:c.1730A>G	XP_011535372.1:p.Gln577Arg
XM_011537071.1:c.1697A>G	XP_011535373.1:p.Gln566Arg
XM_011537072.1:c.1676A>G	XP_011535374.1:p.Gln559Arg
XM_011537073.1:c.1469A>G	XP_011535375.1:p.Gln490Arg
XM_011537074.1:c.1469A>G	XP_011535376.1:p.Gln490Arg
XM_005267991.3:c.1883A>G	XP_005268048.2:p.Gln628Arg
XM_005267992.3:c.1877A>G	XP_005268049.2:p.Gln626Arg
XM_011537067.2:c.1826A>G	XP_011535369.1:p.Gln609Arg
XM_011537069.2:c.1874A>G	XP_011535371.2:p.Gln625Arg
XM_011537070.2:c.1730A>G	XP_011535372.1:p.Gln577Arg
XM_011537071.2:c.1784A>G	XP_011535373.2:p.Gln595Arg
XM_011537072.2:c.1676A>G	XP_011535374.1:p.Gln559Arg
XM_017021582.1:c.1934A>G	XP_016877071.1:p.Gln645Arg
XM_017021583.1:c.1925A>G	XP_016877072.1:p.Gln642Arg
XM_017021584.1:c.1844A>G	XP_016877073.1:p.Gln615Arg
XM_017021585.1:c.1793A>G	XP_016877074.1:p.Gln598Arg
XM_017021586.1:c.1469A>G	XP_016877075.1:p.Gln490Arg
XM_017021587.1:c.1469A>G	XP_016877076.1:p.Gln490Arg
XM_017021588.1:c.1469A>G	XP_016877077.1:p.Gln490Arg
NM_001164749.2:c.1775A>G MANE Select	NP_001158221.1:p.Gln592Arg
NM_001165893.2:c.1685A>G	NP_001159365.1:p.Gln562Arg
NM_022123.3:c.1679A>G	NP_071406.1:p.Gln560Arg
NM_173159.3:c.1736A>G	NP_775182.1:p.Gln579Arg
NM_001394988.1:c.1730A>G	NP_001381917.1:p.Gln577Arg
NM_001394989.1:c.1676A>G	NP_001381918.1:p.Gln559Arg