Canonical Allele Identifier: CA389412552

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269323C>G (hg19) ; chr14:g.33800117C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800117C>G , CM000676.2:g.33800117C>G	GRCh38
NC_000014.8:g.34269323C>G , CM000676.1:g.34269323C>G	GRCh37
NC_000014.7:g.33339074C>G	NCBI36
NG_013036.1:g.865865C>G
NG_013036.2:g.865865C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1810C>G MANE Select	ENSP00000348460.4:p.Arg604Gly
ENST00000551634.6:c.1819C>G	ENSP00000448373.2:p.Arg607Gly
ENST00000680362.1:c.1710C>G
ENST00000681323.1:c.793+2536C>G
ENST00000346562.6:c.1714C>G	ENSP00000319610.5:p.Arg572Gly
ENST00000356141.8:c.1810C>G	ENSP00000348460.4:p.Arg604Gly
ENST00000357798.9:c.1771C>G	ENSP00000350446.5:p.Arg591Gly
ENST00000548645.5:c.1720C>G	ENSP00000448916.1:p.Arg574Gly
ENST00000551492.5:c.1825C>G	ENSP00000450392.1:p.Arg609Gly
ENST00000551634.5:c.1732C>G	ENSP00000448373.1:p.Arg578Gly
NM_001164749.1:c.1810C>G	NP_001158221.1:p.Arg604Gly
NM_001165893.1:c.1720C>G	NP_001159365.1:p.Arg574Gly
NM_022123.2:c.1714C>G	NP_071406.1:p.Arg572Gly
NM_173159.2:c.1771C>G	NP_775182.1:p.Arg591Gly
XM_005267991.2:c.1831C>G	XP_005268048.1:p.Arg611Gly
XM_005267992.2:c.1825C>G	XP_005268049.1:p.Arg609Gly
XM_005267993.2:c.1771C>G	XP_005268050.1:p.Arg591Gly
XM_011537067.1:c.1861C>G	XP_011535369.1:p.Arg621Gly
XM_011537068.1:c.1852C>G	XP_011535370.1:p.Arg618Gly
XM_011537069.1:c.1822C>G	XP_011535371.1:p.Arg608Gly
XM_011537070.1:c.1765C>G	XP_011535372.1:p.Arg589Gly
XM_011537071.1:c.1732C>G	XP_011535373.1:p.Arg578Gly
XM_011537072.1:c.1711C>G	XP_011535374.1:p.Arg571Gly
XM_011537073.1:c.1504C>G	XP_011535375.1:p.Arg502Gly
XM_011537074.1:c.1504C>G	XP_011535376.1:p.Arg502Gly
XM_005267991.3:c.1918C>G	XP_005268048.2:p.Arg640Gly
XM_005267992.3:c.1912C>G	XP_005268049.2:p.Arg638Gly
XM_011537067.2:c.1861C>G	XP_011535369.1:p.Arg621Gly
XM_011537069.2:c.1909C>G	XP_011535371.2:p.Arg637Gly
XM_011537070.2:c.1765C>G	XP_011535372.1:p.Arg589Gly
XM_011537071.2:c.1819C>G	XP_011535373.2:p.Arg607Gly
XM_011537072.2:c.1711C>G	XP_011535374.1:p.Arg571Gly
XM_017021582.1:c.1969C>G	XP_016877071.1:p.Arg657Gly
XM_017021583.1:c.1960C>G	XP_016877072.1:p.Arg654Gly
XM_017021584.1:c.1879C>G	XP_016877073.1:p.Arg627Gly
XM_017021585.1:c.1828C>G	XP_016877074.1:p.Arg610Gly
XM_017021586.1:c.1504C>G	XP_016877075.1:p.Arg502Gly
XM_017021587.1:c.1504C>G	XP_016877076.1:p.Arg502Gly
XM_017021588.1:c.1504C>G	XP_016877077.1:p.Arg502Gly
NM_001164749.2:c.1810C>G MANE Select	NP_001158221.1:p.Arg604Gly
NM_001165893.2:c.1720C>G	NP_001159365.1:p.Arg574Gly
NM_022123.3:c.1714C>G	NP_071406.1:p.Arg572Gly
NM_173159.3:c.1771C>G	NP_775182.1:p.Arg591Gly
NM_001394988.1:c.1765C>G	NP_001381917.1:p.Arg589Gly
NM_001394989.1:c.1711C>G	NP_001381918.1:p.Arg571Gly