Canonical Allele Identifier: CA389412319
Gene: NPAS3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.33800079C>G , CM000676.2:g.33800079C>G GRCh38
NC_000014.8:g.34269285C>G , CM000676.1:g.34269285C>G GRCh37
NC_000014.7:g.33339036C>G NCBI36
NG_013036.1:g.865827C>G
NG_013036.2:g.865827C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356141.9:c.1772C>G MANE Select ENSP00000348460.4:p.Ala591Gly
ENST00000551634.6:c.1781C>G ENSP00000448373.2:p.Ala594Gly
ENST00000680362.1:c.1672C>G
ENST00000681323.1:c.793+2498C>G
ENST00000346562.6:c.1676C>G ENSP00000319610.5:p.Ala559Gly
ENST00000356141.8:c.1772C>G ENSP00000348460.4:p.Ala591Gly
ENST00000357798.9:c.1733C>G ENSP00000350446.5:p.Ala578Gly
ENST00000548645.5:c.1682C>G ENSP00000448916.1:p.Ala561Gly
ENST00000551492.5:c.1787C>G ENSP00000450392.1:p.Ala596Gly
ENST00000551634.5:c.1694C>G ENSP00000448373.1:p.Ala565Gly
NM_001164749.1:c.1772C>G NP_001158221.1:p.Ala591Gly
NM_001165893.1:c.1682C>G NP_001159365.1:p.Ala561Gly
NM_022123.2:c.1676C>G NP_071406.1:p.Ala559Gly
NM_173159.2:c.1733C>G NP_775182.1:p.Ala578Gly
XM_005267991.2:c.1793C>G XP_005268048.1:p.Ala598Gly
XM_005267992.2:c.1787C>G XP_005268049.1:p.Ala596Gly
XM_005267993.2:c.1733C>G XP_005268050.1:p.Ala578Gly
XM_011537067.1:c.1823C>G XP_011535369.1:p.Ala608Gly
XM_011537068.1:c.1814C>G XP_011535370.1:p.Ala605Gly
XM_011537069.1:c.1784C>G XP_011535371.1:p.Ala595Gly
XM_011537070.1:c.1727C>G XP_011535372.1:p.Ala576Gly
XM_011537071.1:c.1694C>G XP_011535373.1:p.Ala565Gly
XM_011537072.1:c.1673C>G XP_011535374.1:p.Ala558Gly
XM_011537073.1:c.1466C>G XP_011535375.1:p.Ala489Gly
XM_011537074.1:c.1466C>G XP_011535376.1:p.Ala489Gly
XM_005267991.3:c.1880C>G XP_005268048.2:p.Ala627Gly
XM_005267992.3:c.1874C>G XP_005268049.2:p.Ala625Gly
XM_011537067.2:c.1823C>G XP_011535369.1:p.Ala608Gly
XM_011537069.2:c.1871C>G XP_011535371.2:p.Ala624Gly
XM_011537070.2:c.1727C>G XP_011535372.1:p.Ala576Gly
XM_011537071.2:c.1781C>G XP_011535373.2:p.Ala594Gly
XM_011537072.2:c.1673C>G XP_011535374.1:p.Ala558Gly
XM_017021582.1:c.1931C>G XP_016877071.1:p.Ala644Gly
XM_017021583.1:c.1922C>G XP_016877072.1:p.Ala641Gly
XM_017021584.1:c.1841C>G XP_016877073.1:p.Ala614Gly
XM_017021585.1:c.1790C>G XP_016877074.1:p.Ala597Gly
XM_017021586.1:c.1466C>G XP_016877075.1:p.Ala489Gly
XM_017021587.1:c.1466C>G XP_016877076.1:p.Ala489Gly
XM_017021588.1:c.1466C>G XP_016877077.1:p.Ala489Gly
NM_001164749.2:c.1772C>G MANE Select NP_001158221.1:p.Ala591Gly
NM_001165893.2:c.1682C>G NP_001159365.1:p.Ala561Gly
NM_022123.3:c.1676C>G NP_071406.1:p.Ala559Gly
NM_173159.3:c.1733C>G NP_775182.1:p.Ala578Gly
NM_001394988.1:c.1727C>G NP_001381917.1:p.Ala576Gly
NM_001394989.1:c.1673C>G NP_001381918.1:p.Ala558Gly