Canonical Allele Identifier: CA486092783
Gene: NPAS3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.34269319A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.33800113A>G , CM000676.2:g.33800113A>G GRCh38
NC_000014.8:g.34269319A>G , CM000676.1:g.34269319A>G GRCh37
NC_000014.7:g.33339070A>G NCBI36
NG_013036.1:g.865861A>G
NG_013036.2:g.865861A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356141.9:c.1806A>G MANE Select ENSP00000348460.4:p.Lys602=
ENST00000551634.6:c.1815A>G ENSP00000448373.2:p.Lys605=
ENST00000680362.1:c.1706A>G
ENST00000681323.1:c.793+2532A>G
ENST00000346562.6:c.1710A>G ENSP00000319610.5:p.Lys570=
ENST00000356141.8:c.1806A>G ENSP00000348460.4:p.Lys602=
ENST00000357798.9:c.1767A>G ENSP00000350446.5:p.Lys589=
ENST00000548645.5:c.1716A>G ENSP00000448916.1:p.Lys572=
ENST00000551492.5:c.1821A>G ENSP00000450392.1:p.Lys607=
ENST00000551634.5:c.1728A>G ENSP00000448373.1:p.Lys576=
NM_001164749.1:c.1806A>G NP_001158221.1:p.Lys602=
NM_001165893.1:c.1716A>G NP_001159365.1:p.Lys572=
NM_022123.2:c.1710A>G NP_071406.1:p.Lys570=
NM_173159.2:c.1767A>G NP_775182.1:p.Lys589=
XM_005267991.2:c.1827A>G XP_005268048.1:p.Lys609=
XM_005267992.2:c.1821A>G XP_005268049.1:p.Lys607=
XM_005267993.2:c.1767A>G XP_005268050.1:p.Lys589=
XM_011537067.1:c.1857A>G XP_011535369.1:p.Lys619=
XM_011537068.1:c.1848A>G XP_011535370.1:p.Lys616=
XM_011537069.1:c.1818A>G XP_011535371.1:p.Lys606=
XM_011537070.1:c.1761A>G XP_011535372.1:p.Lys587=
XM_011537071.1:c.1728A>G XP_011535373.1:p.Lys576=
XM_011537072.1:c.1707A>G XP_011535374.1:p.Lys569=
XM_011537073.1:c.1500A>G XP_011535375.1:p.Lys500=
XM_011537074.1:c.1500A>G XP_011535376.1:p.Lys500=
XM_005267991.3:c.1914A>G XP_005268048.2:p.Lys638=
XM_005267992.3:c.1908A>G XP_005268049.2:p.Lys636=
XM_011537067.2:c.1857A>G XP_011535369.1:p.Lys619=
XM_011537069.2:c.1905A>G XP_011535371.2:p.Lys635=
XM_011537070.2:c.1761A>G XP_011535372.1:p.Lys587=
XM_011537071.2:c.1815A>G XP_011535373.2:p.Lys605=
XM_011537072.2:c.1707A>G XP_011535374.1:p.Lys569=
XM_017021582.1:c.1965A>G XP_016877071.1:p.Lys655=
XM_017021583.1:c.1956A>G XP_016877072.1:p.Lys652=
XM_017021584.1:c.1875A>G XP_016877073.1:p.Lys625=
XM_017021585.1:c.1824A>G XP_016877074.1:p.Lys608=
XM_017021586.1:c.1500A>G XP_016877075.1:p.Lys500=
XM_017021587.1:c.1500A>G XP_016877076.1:p.Lys500=
XM_017021588.1:c.1500A>G XP_016877077.1:p.Lys500=
NM_001164749.2:c.1806A>G MANE Select NP_001158221.1:p.Lys602=
NM_001165893.2:c.1716A>G NP_001159365.1:p.Lys572=
NM_022123.3:c.1710A>G NP_071406.1:p.Lys570=
NM_173159.3:c.1767A>G NP_775182.1:p.Lys589=
NM_001394988.1:c.1761A>G NP_001381917.1:p.Lys587=
NM_001394989.1:c.1707A>G NP_001381918.1:p.Lys569=