Canonical Allele Identifier: CA389413613

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269546C>G (hg19) ; chr14:g.33800340C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800340C>G , CM000676.2:g.33800340C>G	GRCh38
NC_000014.8:g.34269546C>G , CM000676.1:g.34269546C>G	GRCh37
NC_000014.7:g.33339297C>G	NCBI36
NG_013036.1:g.866088C>G
NG_013036.2:g.866088C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2033C>G MANE Select	ENSP00000348460.4:p.Ser678Cys
ENST00000551634.6:c.2042C>G	ENSP00000448373.2:p.Ser681Cys
ENST00000680362.1:c.1933C>G
ENST00000681323.1:c.793+2759C>G
ENST00000346562.6:c.1937C>G	ENSP00000319610.5:p.Ser646Cys
ENST00000356141.8:c.2033C>G	ENSP00000348460.4:p.Ser678Cys
ENST00000357798.9:c.1994C>G	ENSP00000350446.5:p.Ser665Cys
ENST00000548645.5:c.1943C>G	ENSP00000448916.1:p.Ser648Cys
ENST00000551492.5:c.2048C>G	ENSP00000450392.1:p.Ser683Cys
ENST00000551634.5:c.1955C>G	ENSP00000448373.1:p.Ser652Cys
NM_001164749.1:c.2033C>G	NP_001158221.1:p.Ser678Cys
NM_001165893.1:c.1943C>G	NP_001159365.1:p.Ser648Cys
NM_022123.2:c.1937C>G	NP_071406.1:p.Ser646Cys
NM_173159.2:c.1994C>G	NP_775182.1:p.Ser665Cys
XM_005267991.2:c.2054C>G	XP_005268048.1:p.Ser685Cys
XM_005267992.2:c.2048C>G	XP_005268049.1:p.Ser683Cys
XM_005267993.2:c.1994C>G	XP_005268050.1:p.Ser665Cys
XM_011537067.1:c.2084C>G	XP_011535369.1:p.Ser695Cys
XM_011537068.1:c.2075C>G	XP_011535370.1:p.Ser692Cys
XM_011537069.1:c.2045C>G	XP_011535371.1:p.Ser682Cys
XM_011537070.1:c.1988C>G	XP_011535372.1:p.Ser663Cys
XM_011537071.1:c.1955C>G	XP_011535373.1:p.Ser652Cys
XM_011537072.1:c.1934C>G	XP_011535374.1:p.Ser645Cys
XM_011537073.1:c.1727C>G	XP_011535375.1:p.Ser576Cys
XM_011537074.1:c.1727C>G	XP_011535376.1:p.Ser576Cys
XM_005267991.3:c.2141C>G	XP_005268048.2:p.Ser714Cys
XM_005267992.3:c.2135C>G	XP_005268049.2:p.Ser712Cys
XM_011537067.2:c.2084C>G	XP_011535369.1:p.Ser695Cys
XM_011537069.2:c.2132C>G	XP_011535371.2:p.Ser711Cys
XM_011537070.2:c.1988C>G	XP_011535372.1:p.Ser663Cys
XM_011537071.2:c.2042C>G	XP_011535373.2:p.Ser681Cys
XM_011537072.2:c.1934C>G	XP_011535374.1:p.Ser645Cys
XM_017021582.1:c.2192C>G	XP_016877071.1:p.Ser731Cys
XM_017021583.1:c.2183C>G	XP_016877072.1:p.Ser728Cys
XM_017021584.1:c.2102C>G	XP_016877073.1:p.Ser701Cys
XM_017021585.1:c.2051C>G	XP_016877074.1:p.Ser684Cys
XM_017021586.1:c.1727C>G	XP_016877075.1:p.Ser576Cys
XM_017021587.1:c.1727C>G	XP_016877076.1:p.Ser576Cys
XM_017021588.1:c.1727C>G	XP_016877077.1:p.Ser576Cys
NM_001164749.2:c.2033C>G MANE Select	NP_001158221.1:p.Ser678Cys
NM_001165893.2:c.1943C>G	NP_001159365.1:p.Ser648Cys
NM_022123.3:c.1937C>G	NP_071406.1:p.Ser646Cys
NM_173159.3:c.1994C>G	NP_775182.1:p.Ser665Cys
NM_001394988.1:c.1988C>G	NP_001381917.1:p.Ser663Cys
NM_001394989.1:c.1934C>G	NP_001381918.1:p.Ser645Cys