Canonical Allele Identifier: CA389412898

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269379C>G (hg19) ; chr14:g.33800173C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800173C>G , CM000676.2:g.33800173C>G	GRCh38
NC_000014.8:g.34269379C>G , CM000676.1:g.34269379C>G	GRCh37
NC_000014.7:g.33339130C>G	NCBI36
NG_013036.1:g.865921C>G
NG_013036.2:g.865921C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1866C>G MANE Select	ENSP00000348460.4:p.Ser622Arg
ENST00000551634.6:c.1875C>G	ENSP00000448373.2:p.Ser625Arg
ENST00000680362.1:c.1766C>G
ENST00000681323.1:c.793+2592C>G
ENST00000346562.6:c.1770C>G	ENSP00000319610.5:p.Ser590Arg
ENST00000356141.8:c.1866C>G	ENSP00000348460.4:p.Ser622Arg
ENST00000357798.9:c.1827C>G	ENSP00000350446.5:p.Ser609Arg
ENST00000548645.5:c.1776C>G	ENSP00000448916.1:p.Ser592Arg
ENST00000551492.5:c.1881C>G	ENSP00000450392.1:p.Ser627Arg
ENST00000551634.5:c.1788C>G	ENSP00000448373.1:p.Ser596Arg
NM_001164749.1:c.1866C>G	NP_001158221.1:p.Ser622Arg
NM_001165893.1:c.1776C>G	NP_001159365.1:p.Ser592Arg
NM_022123.2:c.1770C>G	NP_071406.1:p.Ser590Arg
NM_173159.2:c.1827C>G	NP_775182.1:p.Ser609Arg
XM_005267991.2:c.1887C>G	XP_005268048.1:p.Ser629Arg
XM_005267992.2:c.1881C>G	XP_005268049.1:p.Ser627Arg
XM_005267993.2:c.1827C>G	XP_005268050.1:p.Ser609Arg
XM_011537067.1:c.1917C>G	XP_011535369.1:p.Ser639Arg
XM_011537068.1:c.1908C>G	XP_011535370.1:p.Ser636Arg
XM_011537069.1:c.1878C>G	XP_011535371.1:p.Ser626Arg
XM_011537070.1:c.1821C>G	XP_011535372.1:p.Ser607Arg
XM_011537071.1:c.1788C>G	XP_011535373.1:p.Ser596Arg
XM_011537072.1:c.1767C>G	XP_011535374.1:p.Ser589Arg
XM_011537073.1:c.1560C>G	XP_011535375.1:p.Ser520Arg
XM_011537074.1:c.1560C>G	XP_011535376.1:p.Ser520Arg
XM_005267991.3:c.1974C>G	XP_005268048.2:p.Ser658Arg
XM_005267992.3:c.1968C>G	XP_005268049.2:p.Ser656Arg
XM_011537067.2:c.1917C>G	XP_011535369.1:p.Ser639Arg
XM_011537069.2:c.1965C>G	XP_011535371.2:p.Ser655Arg
XM_011537070.2:c.1821C>G	XP_011535372.1:p.Ser607Arg
XM_011537071.2:c.1875C>G	XP_011535373.2:p.Ser625Arg
XM_011537072.2:c.1767C>G	XP_011535374.1:p.Ser589Arg
XM_017021582.1:c.2025C>G	XP_016877071.1:p.Ser675Arg
XM_017021583.1:c.2016C>G	XP_016877072.1:p.Ser672Arg
XM_017021584.1:c.1935C>G	XP_016877073.1:p.Ser645Arg
XM_017021585.1:c.1884C>G	XP_016877074.1:p.Ser628Arg
XM_017021586.1:c.1560C>G	XP_016877075.1:p.Ser520Arg
XM_017021587.1:c.1560C>G	XP_016877076.1:p.Ser520Arg
XM_017021588.1:c.1560C>G	XP_016877077.1:p.Ser520Arg
NM_001164749.2:c.1866C>G MANE Select	NP_001158221.1:p.Ser622Arg
NM_001165893.2:c.1776C>G	NP_001159365.1:p.Ser592Arg
NM_022123.3:c.1770C>G	NP_071406.1:p.Ser590Arg
NM_173159.3:c.1827C>G	NP_775182.1:p.Ser609Arg
NM_001394988.1:c.1821C>G	NP_001381917.1:p.Ser607Arg
NM_001394989.1:c.1767C>G	NP_001381918.1:p.Ser589Arg