Canonical Allele Identifier: CA389412142

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269255A>T (hg19) ; chr14:g.33800049A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800049A>T , CM000676.2:g.33800049A>T	GRCh38
NC_000014.8:g.34269255A>T , CM000676.1:g.34269255A>T	GRCh37
NC_000014.7:g.33339006A>T	NCBI36
NG_013036.1:g.865797A>T
NG_013036.2:g.865797A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1742A>T MANE Select	ENSP00000348460.4:p.Lys581Met
ENST00000551634.6:c.1751A>T	ENSP00000448373.2:p.Lys584Met
ENST00000680362.1:c.1642A>T
ENST00000681323.1:c.793+2468A>T
ENST00000346562.6:c.1646A>T	ENSP00000319610.5:p.Lys549Met
ENST00000356141.8:c.1742A>T	ENSP00000348460.4:p.Lys581Met
ENST00000357798.9:c.1703A>T	ENSP00000350446.5:p.Lys568Met
ENST00000548645.5:c.1652A>T	ENSP00000448916.1:p.Lys551Met
ENST00000551492.5:c.1757A>T	ENSP00000450392.1:p.Lys586Met
ENST00000551634.5:c.1664A>T	ENSP00000448373.1:p.Lys555Met
NM_001164749.1:c.1742A>T	NP_001158221.1:p.Lys581Met
NM_001165893.1:c.1652A>T	NP_001159365.1:p.Lys551Met
NM_022123.2:c.1646A>T	NP_071406.1:p.Lys549Met
NM_173159.2:c.1703A>T	NP_775182.1:p.Lys568Met
XM_005267991.2:c.1763A>T	XP_005268048.1:p.Lys588Met
XM_005267992.2:c.1757A>T	XP_005268049.1:p.Lys586Met
XM_005267993.2:c.1703A>T	XP_005268050.1:p.Lys568Met
XM_011537067.1:c.1793A>T	XP_011535369.1:p.Lys598Met
XM_011537068.1:c.1784A>T	XP_011535370.1:p.Lys595Met
XM_011537069.1:c.1754A>T	XP_011535371.1:p.Lys585Met
XM_011537070.1:c.1697A>T	XP_011535372.1:p.Lys566Met
XM_011537071.1:c.1664A>T	XP_011535373.1:p.Lys555Met
XM_011537072.1:c.1643A>T	XP_011535374.1:p.Lys548Met
XM_011537073.1:c.1436A>T	XP_011535375.1:p.Lys479Met
XM_011537074.1:c.1436A>T	XP_011535376.1:p.Lys479Met
XM_005267991.3:c.1850A>T	XP_005268048.2:p.Lys617Met
XM_005267992.3:c.1844A>T	XP_005268049.2:p.Lys615Met
XM_011537067.2:c.1793A>T	XP_011535369.1:p.Lys598Met
XM_011537069.2:c.1841A>T	XP_011535371.2:p.Lys614Met
XM_011537070.2:c.1697A>T	XP_011535372.1:p.Lys566Met
XM_011537071.2:c.1751A>T	XP_011535373.2:p.Lys584Met
XM_011537072.2:c.1643A>T	XP_011535374.1:p.Lys548Met
XM_017021582.1:c.1901A>T	XP_016877071.1:p.Lys634Met
XM_017021583.1:c.1892A>T	XP_016877072.1:p.Lys631Met
XM_017021584.1:c.1811A>T	XP_016877073.1:p.Lys604Met
XM_017021585.1:c.1760A>T	XP_016877074.1:p.Lys587Met
XM_017021586.1:c.1436A>T	XP_016877075.1:p.Lys479Met
XM_017021587.1:c.1436A>T	XP_016877076.1:p.Lys479Met
XM_017021588.1:c.1436A>T	XP_016877077.1:p.Lys479Met
NM_001164749.2:c.1742A>T MANE Select	NP_001158221.1:p.Lys581Met
NM_001165893.2:c.1652A>T	NP_001159365.1:p.Lys551Met
NM_022123.3:c.1646A>T	NP_071406.1:p.Lys549Met
NM_173159.3:c.1703A>T	NP_775182.1:p.Lys568Met
NM_001394988.1:c.1697A>T	NP_001381917.1:p.Lys566Met
NM_001394989.1:c.1643A>T	NP_001381918.1:p.Lys548Met