Canonical Allele Identifier: CA389412978

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269399G>T (hg19) ; chr14:g.33800193G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800193G>T , CM000676.2:g.33800193G>T	GRCh38
NC_000014.8:g.34269399G>T , CM000676.1:g.34269399G>T	GRCh37
NC_000014.7:g.33339150G>T	NCBI36
NG_013036.1:g.865941G>T
NG_013036.2:g.865941G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1886G>T MANE Select	ENSP00000348460.4:p.Gly629Val
ENST00000551634.6:c.1895G>T	ENSP00000448373.2:p.Gly632Val
ENST00000680362.1:c.1786G>T
ENST00000681323.1:c.793+2612G>T
ENST00000346562.6:c.1790G>T	ENSP00000319610.5:p.Gly597Val
ENST00000356141.8:c.1886G>T	ENSP00000348460.4:p.Gly629Val
ENST00000357798.9:c.1847G>T	ENSP00000350446.5:p.Gly616Val
ENST00000548645.5:c.1796G>T	ENSP00000448916.1:p.Gly599Val
ENST00000551492.5:c.1901G>T	ENSP00000450392.1:p.Gly634Val
ENST00000551634.5:c.1808G>T	ENSP00000448373.1:p.Gly603Val
NM_001164749.1:c.1886G>T	NP_001158221.1:p.Gly629Val
NM_001165893.1:c.1796G>T	NP_001159365.1:p.Gly599Val
NM_022123.2:c.1790G>T	NP_071406.1:p.Gly597Val
NM_173159.2:c.1847G>T	NP_775182.1:p.Gly616Val
XM_005267991.2:c.1907G>T	XP_005268048.1:p.Gly636Val
XM_005267992.2:c.1901G>T	XP_005268049.1:p.Gly634Val
XM_005267993.2:c.1847G>T	XP_005268050.1:p.Gly616Val
XM_011537067.1:c.1937G>T	XP_011535369.1:p.Gly646Val
XM_011537068.1:c.1928G>T	XP_011535370.1:p.Gly643Val
XM_011537069.1:c.1898G>T	XP_011535371.1:p.Gly633Val
XM_011537070.1:c.1841G>T	XP_011535372.1:p.Gly614Val
XM_011537071.1:c.1808G>T	XP_011535373.1:p.Gly603Val
XM_011537072.1:c.1787G>T	XP_011535374.1:p.Gly596Val
XM_011537073.1:c.1580G>T	XP_011535375.1:p.Gly527Val
XM_011537074.1:c.1580G>T	XP_011535376.1:p.Gly527Val
XM_005267991.3:c.1994G>T	XP_005268048.2:p.Gly665Val
XM_005267992.3:c.1988G>T	XP_005268049.2:p.Gly663Val
XM_011537067.2:c.1937G>T	XP_011535369.1:p.Gly646Val
XM_011537069.2:c.1985G>T	XP_011535371.2:p.Gly662Val
XM_011537070.2:c.1841G>T	XP_011535372.1:p.Gly614Val
XM_011537071.2:c.1895G>T	XP_011535373.2:p.Gly632Val
XM_011537072.2:c.1787G>T	XP_011535374.1:p.Gly596Val
XM_017021582.1:c.2045G>T	XP_016877071.1:p.Gly682Val
XM_017021583.1:c.2036G>T	XP_016877072.1:p.Gly679Val
XM_017021584.1:c.1955G>T	XP_016877073.1:p.Gly652Val
XM_017021585.1:c.1904G>T	XP_016877074.1:p.Gly635Val
XM_017021586.1:c.1580G>T	XP_016877075.1:p.Gly527Val
XM_017021587.1:c.1580G>T	XP_016877076.1:p.Gly527Val
XM_017021588.1:c.1580G>T	XP_016877077.1:p.Gly527Val
NM_001164749.2:c.1886G>T MANE Select	NP_001158221.1:p.Gly629Val
NM_001165893.2:c.1796G>T	NP_001159365.1:p.Gly599Val
NM_022123.3:c.1790G>T	NP_071406.1:p.Gly597Val
NM_173159.3:c.1847G>T	NP_775182.1:p.Gly616Val
NM_001394988.1:c.1841G>T	NP_001381917.1:p.Gly614Val
NM_001394989.1:c.1787G>T	NP_001381918.1:p.Gly596Val