Canonical Allele Identifier: CA486092830

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269356C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800150C>A , CM000676.2:g.33800150C>A	GRCh38
NC_000014.8:g.34269356C>A , CM000676.1:g.34269356C>A	GRCh37
NC_000014.7:g.33339107C>A	NCBI36
NG_013036.1:g.865898C>A
NG_013036.2:g.865898C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1843C>A MANE Select	ENSP00000348460.4:p.Arg615=
ENST00000551634.6:c.1852C>A	ENSP00000448373.2:p.Arg618=
ENST00000680362.1:c.1743C>A
ENST00000681323.1:c.793+2569C>A
ENST00000346562.6:c.1747C>A	ENSP00000319610.5:p.Arg583=
ENST00000356141.8:c.1843C>A	ENSP00000348460.4:p.Arg615=
ENST00000357798.9:c.1804C>A	ENSP00000350446.5:p.Arg602=
ENST00000548645.5:c.1753C>A	ENSP00000448916.1:p.Arg585=
ENST00000551492.5:c.1858C>A	ENSP00000450392.1:p.Arg620=
ENST00000551634.5:c.1765C>A	ENSP00000448373.1:p.Arg589=
NM_001164749.1:c.1843C>A	NP_001158221.1:p.Arg615=
NM_001165893.1:c.1753C>A	NP_001159365.1:p.Arg585=
NM_022123.2:c.1747C>A	NP_071406.1:p.Arg583=
NM_173159.2:c.1804C>A	NP_775182.1:p.Arg602=
XM_005267991.2:c.1864C>A	XP_005268048.1:p.Arg622=
XM_005267992.2:c.1858C>A	XP_005268049.1:p.Arg620=
XM_005267993.2:c.1804C>A	XP_005268050.1:p.Arg602=
XM_011537067.1:c.1894C>A	XP_011535369.1:p.Arg632=
XM_011537068.1:c.1885C>A	XP_011535370.1:p.Arg629=
XM_011537069.1:c.1855C>A	XP_011535371.1:p.Arg619=
XM_011537070.1:c.1798C>A	XP_011535372.1:p.Arg600=
XM_011537071.1:c.1765C>A	XP_011535373.1:p.Arg589=
XM_011537072.1:c.1744C>A	XP_011535374.1:p.Arg582=
XM_011537073.1:c.1537C>A	XP_011535375.1:p.Arg513=
XM_011537074.1:c.1537C>A	XP_011535376.1:p.Arg513=
XM_005267991.3:c.1951C>A	XP_005268048.2:p.Arg651=
XM_005267992.3:c.1945C>A	XP_005268049.2:p.Arg649=
XM_011537067.2:c.1894C>A	XP_011535369.1:p.Arg632=
XM_011537069.2:c.1942C>A	XP_011535371.2:p.Arg648=
XM_011537070.2:c.1798C>A	XP_011535372.1:p.Arg600=
XM_011537071.2:c.1852C>A	XP_011535373.2:p.Arg618=
XM_011537072.2:c.1744C>A	XP_011535374.1:p.Arg582=
XM_017021582.1:c.2002C>A	XP_016877071.1:p.Arg668=
XM_017021583.1:c.1993C>A	XP_016877072.1:p.Arg665=
XM_017021584.1:c.1912C>A	XP_016877073.1:p.Arg638=
XM_017021585.1:c.1861C>A	XP_016877074.1:p.Arg621=
XM_017021586.1:c.1537C>A	XP_016877075.1:p.Arg513=
XM_017021587.1:c.1537C>A	XP_016877076.1:p.Arg513=
XM_017021588.1:c.1537C>A	XP_016877077.1:p.Arg513=
NM_001164749.2:c.1843C>A MANE Select	NP_001158221.1:p.Arg615=
NM_001165893.2:c.1753C>A	NP_001159365.1:p.Arg585=
NM_022123.3:c.1747C>A	NP_071406.1:p.Arg583=
NM_173159.3:c.1804C>A	NP_775182.1:p.Arg602=
NM_001394988.1:c.1798C>A	NP_001381917.1:p.Arg600=
NM_001394989.1:c.1744C>A	NP_001381918.1:p.Arg582=