Canonical Allele Identifier: CA389412134

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269254A>T (hg19) ; chr14:g.33800048A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800048A>T , CM000676.2:g.33800048A>T	GRCh38
NC_000014.8:g.34269254A>T , CM000676.1:g.34269254A>T	GRCh37
NC_000014.7:g.33339005A>T	NCBI36
NG_013036.1:g.865796A>T
NG_013036.2:g.865796A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1741A>T MANE Select	ENSP00000348460.4:p.Lys581Ter
ENST00000551634.6:c.1750A>T	ENSP00000448373.2:p.Lys584Ter
ENST00000680362.1:c.1641A>T
ENST00000681323.1:c.793+2467A>T
ENST00000346562.6:c.1645A>T	ENSP00000319610.5:p.Lys549Ter
ENST00000356141.8:c.1741A>T	ENSP00000348460.4:p.Lys581Ter
ENST00000357798.9:c.1702A>T	ENSP00000350446.5:p.Lys568Ter
ENST00000548645.5:c.1651A>T	ENSP00000448916.1:p.Lys551Ter
ENST00000551492.5:c.1756A>T	ENSP00000450392.1:p.Lys586Ter
ENST00000551634.5:c.1663A>T	ENSP00000448373.1:p.Lys555Ter
NM_001164749.1:c.1741A>T	NP_001158221.1:p.Lys581Ter
NM_001165893.1:c.1651A>T	NP_001159365.1:p.Lys551Ter
NM_022123.2:c.1645A>T	NP_071406.1:p.Lys549Ter
NM_173159.2:c.1702A>T	NP_775182.1:p.Lys568Ter
XM_005267991.2:c.1762A>T	XP_005268048.1:p.Lys588Ter
XM_005267992.2:c.1756A>T	XP_005268049.1:p.Lys586Ter
XM_005267993.2:c.1702A>T	XP_005268050.1:p.Lys568Ter
XM_011537067.1:c.1792A>T	XP_011535369.1:p.Lys598Ter
XM_011537068.1:c.1783A>T	XP_011535370.1:p.Lys595Ter
XM_011537069.1:c.1753A>T	XP_011535371.1:p.Lys585Ter
XM_011537070.1:c.1696A>T	XP_011535372.1:p.Lys566Ter
XM_011537071.1:c.1663A>T	XP_011535373.1:p.Lys555Ter
XM_011537072.1:c.1642A>T	XP_011535374.1:p.Lys548Ter
XM_011537073.1:c.1435A>T	XP_011535375.1:p.Lys479Ter
XM_011537074.1:c.1435A>T	XP_011535376.1:p.Lys479Ter
XM_005267991.3:c.1849A>T	XP_005268048.2:p.Lys617Ter
XM_005267992.3:c.1843A>T	XP_005268049.2:p.Lys615Ter
XM_011537067.2:c.1792A>T	XP_011535369.1:p.Lys598Ter
XM_011537069.2:c.1840A>T	XP_011535371.2:p.Lys614Ter
XM_011537070.2:c.1696A>T	XP_011535372.1:p.Lys566Ter
XM_011537071.2:c.1750A>T	XP_011535373.2:p.Lys584Ter
XM_011537072.2:c.1642A>T	XP_011535374.1:p.Lys548Ter
XM_017021582.1:c.1900A>T	XP_016877071.1:p.Lys634Ter
XM_017021583.1:c.1891A>T	XP_016877072.1:p.Lys631Ter
XM_017021584.1:c.1810A>T	XP_016877073.1:p.Lys604Ter
XM_017021585.1:c.1759A>T	XP_016877074.1:p.Lys587Ter
XM_017021586.1:c.1435A>T	XP_016877075.1:p.Lys479Ter
XM_017021587.1:c.1435A>T	XP_016877076.1:p.Lys479Ter
XM_017021588.1:c.1435A>T	XP_016877077.1:p.Lys479Ter
NM_001164749.2:c.1741A>T MANE Select	NP_001158221.1:p.Lys581Ter
NM_001165893.2:c.1651A>T	NP_001159365.1:p.Lys551Ter
NM_022123.3:c.1645A>T	NP_071406.1:p.Lys549Ter
NM_173159.3:c.1702A>T	NP_775182.1:p.Lys568Ter
NM_001394988.1:c.1696A>T	NP_001381917.1:p.Lys566Ter
NM_001394989.1:c.1642A>T	NP_001381918.1:p.Lys548Ter