Canonical Allele Identifier: CA389412135

Gene: NPAS3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1741A>C MANE Select	ENSP00000348460.4:p.Lys581Gln
ENST00000551634.6:c.1750A>C	ENSP00000448373.2:p.Lys584Gln
ENST00000680362.1:c.1641A>C
ENST00000681323.1:c.793+2467A>C
ENST00000346562.6:c.1645A>C	ENSP00000319610.5:p.Lys549Gln
ENST00000356141.8:c.1741A>C	ENSP00000348460.4:p.Lys581Gln
ENST00000357798.9:c.1702A>C	ENSP00000350446.5:p.Lys568Gln
ENST00000548645.5:c.1651A>C	ENSP00000448916.1:p.Lys551Gln
ENST00000551492.5:c.1756A>C	ENSP00000450392.1:p.Lys586Gln
ENST00000551634.5:c.1663A>C	ENSP00000448373.1:p.Lys555Gln
NM_001164749.1:c.1741A>C	NP_001158221.1:p.Lys581Gln
NM_001165893.1:c.1651A>C	NP_001159365.1:p.Lys551Gln
NM_022123.2:c.1645A>C	NP_071406.1:p.Lys549Gln
NM_173159.2:c.1702A>C	NP_775182.1:p.Lys568Gln
XM_005267991.2:c.1762A>C	XP_005268048.1:p.Lys588Gln
XM_005267992.2:c.1756A>C	XP_005268049.1:p.Lys586Gln
XM_005267993.2:c.1702A>C	XP_005268050.1:p.Lys568Gln
XM_011537067.1:c.1792A>C	XP_011535369.1:p.Lys598Gln
XM_011537068.1:c.1783A>C	XP_011535370.1:p.Lys595Gln
XM_011537069.1:c.1753A>C	XP_011535371.1:p.Lys585Gln
XM_011537070.1:c.1696A>C	XP_011535372.1:p.Lys566Gln
XM_011537071.1:c.1663A>C	XP_011535373.1:p.Lys555Gln
XM_011537072.1:c.1642A>C	XP_011535374.1:p.Lys548Gln
XM_011537073.1:c.1435A>C	XP_011535375.1:p.Lys479Gln
XM_011537074.1:c.1435A>C	XP_011535376.1:p.Lys479Gln
XM_005267991.3:c.1849A>C	XP_005268048.2:p.Lys617Gln
XM_005267992.3:c.1843A>C	XP_005268049.2:p.Lys615Gln
XM_011537067.2:c.1792A>C	XP_011535369.1:p.Lys598Gln
XM_011537069.2:c.1840A>C	XP_011535371.2:p.Lys614Gln
XM_011537070.2:c.1696A>C	XP_011535372.1:p.Lys566Gln
XM_011537071.2:c.1750A>C	XP_011535373.2:p.Lys584Gln
XM_011537072.2:c.1642A>C	XP_011535374.1:p.Lys548Gln
XM_017021582.1:c.1900A>C	XP_016877071.1:p.Lys634Gln
XM_017021583.1:c.1891A>C	XP_016877072.1:p.Lys631Gln
XM_017021584.1:c.1810A>C	XP_016877073.1:p.Lys604Gln
XM_017021585.1:c.1759A>C	XP_016877074.1:p.Lys587Gln
XM_017021586.1:c.1435A>C	XP_016877075.1:p.Lys479Gln
XM_017021587.1:c.1435A>C	XP_016877076.1:p.Lys479Gln
XM_017021588.1:c.1435A>C	XP_016877077.1:p.Lys479Gln
NM_001164749.2:c.1741A>C MANE Select	NP_001158221.1:p.Lys581Gln
NM_001165893.2:c.1651A>C	NP_001159365.1:p.Lys551Gln
NM_022123.3:c.1645A>C	NP_071406.1:p.Lys549Gln
NM_173159.3:c.1702A>C	NP_775182.1:p.Lys568Gln
NM_001394988.1:c.1696A>C	NP_001381917.1:p.Lys566Gln
NM_001394989.1:c.1642A>C	NP_001381918.1:p.Lys548Gln