Canonical Allele Identifier: CA389414151

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269695A>T (hg19) ; chr14:g.33800489A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800489A>T , CM000676.2:g.33800489A>T	GRCh38
NC_000014.8:g.34269695A>T , CM000676.1:g.34269695A>T	GRCh37
NC_000014.7:g.33339446A>T	NCBI36
NG_013036.1:g.866237A>T
NG_013036.2:g.866237A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2182A>T MANE Select	ENSP00000348460.4:p.Lys728Ter
ENST00000551634.6:c.2191A>T	ENSP00000448373.2:p.Lys731Ter
ENST00000680362.1:c.2082A>T
ENST00000681323.1:c.793+2908A>T
ENST00000346562.6:c.2086A>T	ENSP00000319610.5:p.Lys696Ter
ENST00000356141.8:c.2182A>T	ENSP00000348460.4:p.Lys728Ter
ENST00000357798.9:c.2143A>T	ENSP00000350446.5:p.Lys715Ter
ENST00000548645.5:c.2092A>T	ENSP00000448916.1:p.Lys698Ter
ENST00000551492.5:c.2197A>T	ENSP00000450392.1:p.Lys733Ter
ENST00000551634.5:c.2104A>T	ENSP00000448373.1:p.Lys702Ter
NM_001164749.1:c.2182A>T	NP_001158221.1:p.Lys728Ter
NM_001165893.1:c.2092A>T	NP_001159365.1:p.Lys698Ter
NM_022123.2:c.2086A>T	NP_071406.1:p.Lys696Ter
NM_173159.2:c.2143A>T	NP_775182.1:p.Lys715Ter
XM_005267991.2:c.2203A>T	XP_005268048.1:p.Lys735Ter
XM_005267992.2:c.2197A>T	XP_005268049.1:p.Lys733Ter
XM_005267993.2:c.2143A>T	XP_005268050.1:p.Lys715Ter
XM_011537067.1:c.2233A>T	XP_011535369.1:p.Lys745Ter
XM_011537068.1:c.2224A>T	XP_011535370.1:p.Lys742Ter
XM_011537069.1:c.2194A>T	XP_011535371.1:p.Lys732Ter
XM_011537070.1:c.2137A>T	XP_011535372.1:p.Lys713Ter
XM_011537071.1:c.2104A>T	XP_011535373.1:p.Lys702Ter
XM_011537072.1:c.2083A>T	XP_011535374.1:p.Lys695Ter
XM_011537073.1:c.1876A>T	XP_011535375.1:p.Lys626Ter
XM_011537074.1:c.1876A>T	XP_011535376.1:p.Lys626Ter
XM_005267991.3:c.2290A>T	XP_005268048.2:p.Lys764Ter
XM_005267992.3:c.2284A>T	XP_005268049.2:p.Lys762Ter
XM_011537067.2:c.2233A>T	XP_011535369.1:p.Lys745Ter
XM_011537069.2:c.2281A>T	XP_011535371.2:p.Lys761Ter
XM_011537070.2:c.2137A>T	XP_011535372.1:p.Lys713Ter
XM_011537071.2:c.2191A>T	XP_011535373.2:p.Lys731Ter
XM_011537072.2:c.2083A>T	XP_011535374.1:p.Lys695Ter
XM_017021582.1:c.2341A>T	XP_016877071.1:p.Lys781Ter
XM_017021583.1:c.2332A>T	XP_016877072.1:p.Lys778Ter
XM_017021584.1:c.2251A>T	XP_016877073.1:p.Lys751Ter
XM_017021585.1:c.2200A>T	XP_016877074.1:p.Lys734Ter
XM_017021586.1:c.1876A>T	XP_016877075.1:p.Lys626Ter
XM_017021587.1:c.1876A>T	XP_016877076.1:p.Lys626Ter
XM_017021588.1:c.1876A>T	XP_016877077.1:p.Lys626Ter
NM_001164749.2:c.2182A>T MANE Select	NP_001158221.1:p.Lys728Ter
NM_001165893.2:c.2092A>T	NP_001159365.1:p.Lys698Ter
NM_022123.3:c.2086A>T	NP_071406.1:p.Lys696Ter
NM_173159.3:c.2143A>T	NP_775182.1:p.Lys715Ter
NM_001394988.1:c.2137A>T	NP_001381917.1:p.Lys713Ter
NM_001394989.1:c.2083A>T	NP_001381918.1:p.Lys695Ter