Canonical Allele Identifier: CA389412814
Gene: NPAS3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.33800157T>C , CM000676.2:g.33800157T>C GRCh38
NC_000014.8:g.34269363T>C , CM000676.1:g.34269363T>C GRCh37
NC_000014.7:g.33339114T>C NCBI36
NG_013036.1:g.865905T>C
NG_013036.2:g.865905T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356141.9:c.1850T>C MANE Select ENSP00000348460.4:p.Leu617Pro
ENST00000551634.6:c.1859T>C ENSP00000448373.2:p.Leu620Pro
ENST00000680362.1:c.1750T>C
ENST00000681323.1:c.793+2576T>C
ENST00000346562.6:c.1754T>C ENSP00000319610.5:p.Leu585Pro
ENST00000356141.8:c.1850T>C ENSP00000348460.4:p.Leu617Pro
ENST00000357798.9:c.1811T>C ENSP00000350446.5:p.Leu604Pro
ENST00000548645.5:c.1760T>C ENSP00000448916.1:p.Leu587Pro
ENST00000551492.5:c.1865T>C ENSP00000450392.1:p.Leu622Pro
ENST00000551634.5:c.1772T>C ENSP00000448373.1:p.Leu591Pro
NM_001164749.1:c.1850T>C NP_001158221.1:p.Leu617Pro
NM_001165893.1:c.1760T>C NP_001159365.1:p.Leu587Pro
NM_022123.2:c.1754T>C NP_071406.1:p.Leu585Pro
NM_173159.2:c.1811T>C NP_775182.1:p.Leu604Pro
XM_005267991.2:c.1871T>C XP_005268048.1:p.Leu624Pro
XM_005267992.2:c.1865T>C XP_005268049.1:p.Leu622Pro
XM_005267993.2:c.1811T>C XP_005268050.1:p.Leu604Pro
XM_011537067.1:c.1901T>C XP_011535369.1:p.Leu634Pro
XM_011537068.1:c.1892T>C XP_011535370.1:p.Leu631Pro
XM_011537069.1:c.1862T>C XP_011535371.1:p.Leu621Pro
XM_011537070.1:c.1805T>C XP_011535372.1:p.Leu602Pro
XM_011537071.1:c.1772T>C XP_011535373.1:p.Leu591Pro
XM_011537072.1:c.1751T>C XP_011535374.1:p.Leu584Pro
XM_011537073.1:c.1544T>C XP_011535375.1:p.Leu515Pro
XM_011537074.1:c.1544T>C XP_011535376.1:p.Leu515Pro
XM_005267991.3:c.1958T>C XP_005268048.2:p.Leu653Pro
XM_005267992.3:c.1952T>C XP_005268049.2:p.Leu651Pro
XM_011537067.2:c.1901T>C XP_011535369.1:p.Leu634Pro
XM_011537069.2:c.1949T>C XP_011535371.2:p.Leu650Pro
XM_011537070.2:c.1805T>C XP_011535372.1:p.Leu602Pro
XM_011537071.2:c.1859T>C XP_011535373.2:p.Leu620Pro
XM_011537072.2:c.1751T>C XP_011535374.1:p.Leu584Pro
XM_017021582.1:c.2009T>C XP_016877071.1:p.Leu670Pro
XM_017021583.1:c.2000T>C XP_016877072.1:p.Leu667Pro
XM_017021584.1:c.1919T>C XP_016877073.1:p.Leu640Pro
XM_017021585.1:c.1868T>C XP_016877074.1:p.Leu623Pro
XM_017021586.1:c.1544T>C XP_016877075.1:p.Leu515Pro
XM_017021587.1:c.1544T>C XP_016877076.1:p.Leu515Pro
XM_017021588.1:c.1544T>C XP_016877077.1:p.Leu515Pro
NM_001164749.2:c.1850T>C MANE Select NP_001158221.1:p.Leu617Pro
NM_001165893.2:c.1760T>C NP_001159365.1:p.Leu587Pro
NM_022123.3:c.1754T>C NP_071406.1:p.Leu585Pro
NM_173159.3:c.1811T>C NP_775182.1:p.Leu604Pro
NM_001394988.1:c.1805T>C NP_001381917.1:p.Leu602Pro
NM_001394989.1:c.1751T>C NP_001381918.1:p.Leu584Pro