Canonical Allele Identifier: CA389413154

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269444C>G (hg19) ; chr14:g.33800238C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800238C>G , CM000676.2:g.33800238C>G	GRCh38
NC_000014.8:g.34269444C>G , CM000676.1:g.34269444C>G	GRCh37
NC_000014.7:g.33339195C>G	NCBI36
NG_013036.1:g.865986C>G
NG_013036.2:g.865986C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1931C>G MANE Select	ENSP00000348460.4:p.Ser644Trp
ENST00000551634.6:c.1940C>G	ENSP00000448373.2:p.Ser647Trp
ENST00000680362.1:c.1831C>G
ENST00000681323.1:c.793+2657C>G
ENST00000346562.6:c.1835C>G	ENSP00000319610.5:p.Ser612Trp
ENST00000356141.8:c.1931C>G	ENSP00000348460.4:p.Ser644Trp
ENST00000357798.9:c.1892C>G	ENSP00000350446.5:p.Ser631Trp
ENST00000548645.5:c.1841C>G	ENSP00000448916.1:p.Ser614Trp
ENST00000551492.5:c.1946C>G	ENSP00000450392.1:p.Ser649Trp
ENST00000551634.5:c.1853C>G	ENSP00000448373.1:p.Ser618Trp
NM_001164749.1:c.1931C>G	NP_001158221.1:p.Ser644Trp
NM_001165893.1:c.1841C>G	NP_001159365.1:p.Ser614Trp
NM_022123.2:c.1835C>G	NP_071406.1:p.Ser612Trp
NM_173159.2:c.1892C>G	NP_775182.1:p.Ser631Trp
XM_005267991.2:c.1952C>G	XP_005268048.1:p.Ser651Trp
XM_005267992.2:c.1946C>G	XP_005268049.1:p.Ser649Trp
XM_005267993.2:c.1892C>G	XP_005268050.1:p.Ser631Trp
XM_011537067.1:c.1982C>G	XP_011535369.1:p.Ser661Trp
XM_011537068.1:c.1973C>G	XP_011535370.1:p.Ser658Trp
XM_011537069.1:c.1943C>G	XP_011535371.1:p.Ser648Trp
XM_011537070.1:c.1886C>G	XP_011535372.1:p.Ser629Trp
XM_011537071.1:c.1853C>G	XP_011535373.1:p.Ser618Trp
XM_011537072.1:c.1832C>G	XP_011535374.1:p.Ser611Trp
XM_011537073.1:c.1625C>G	XP_011535375.1:p.Ser542Trp
XM_011537074.1:c.1625C>G	XP_011535376.1:p.Ser542Trp
XM_005267991.3:c.2039C>G	XP_005268048.2:p.Ser680Trp
XM_005267992.3:c.2033C>G	XP_005268049.2:p.Ser678Trp
XM_011537067.2:c.1982C>G	XP_011535369.1:p.Ser661Trp
XM_011537069.2:c.2030C>G	XP_011535371.2:p.Ser677Trp
XM_011537070.2:c.1886C>G	XP_011535372.1:p.Ser629Trp
XM_011537071.2:c.1940C>G	XP_011535373.2:p.Ser647Trp
XM_011537072.2:c.1832C>G	XP_011535374.1:p.Ser611Trp
XM_017021582.1:c.2090C>G	XP_016877071.1:p.Ser697Trp
XM_017021583.1:c.2081C>G	XP_016877072.1:p.Ser694Trp
XM_017021584.1:c.2000C>G	XP_016877073.1:p.Ser667Trp
XM_017021585.1:c.1949C>G	XP_016877074.1:p.Ser650Trp
XM_017021586.1:c.1625C>G	XP_016877075.1:p.Ser542Trp
XM_017021587.1:c.1625C>G	XP_016877076.1:p.Ser542Trp
XM_017021588.1:c.1625C>G	XP_016877077.1:p.Ser542Trp
NM_001164749.2:c.1931C>G MANE Select	NP_001158221.1:p.Ser644Trp
NM_001165893.2:c.1841C>G	NP_001159365.1:p.Ser614Trp
NM_022123.3:c.1835C>G	NP_071406.1:p.Ser612Trp
NM_173159.3:c.1892C>G	NP_775182.1:p.Ser631Trp
NM_001394988.1:c.1886C>G	NP_001381917.1:p.Ser629Trp
NM_001394989.1:c.1832C>G	NP_001381918.1:p.Ser611Trp