Canonical Allele Identifier: CA389412743

Gene: NPAS3

Linked Data

• dbSNP Id: rs1326364155
• COSMIC: COSM4803157 ; COSM4803158 ; COSM4803159
• MyVariant Identifiers: chr14:g.34269351G>C (hg19) ; chr14:g.33800145G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800145G>C , CM000676.2:g.33800145G>C	GRCh38
NC_000014.8:g.34269351G>C , CM000676.1:g.34269351G>C	GRCh37
NC_000014.7:g.33339102G>C	NCBI36
NG_013036.1:g.865893G>C
NG_013036.2:g.865893G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1838G>C MANE Select	ENSP00000348460.4:p.Ser613Thr
ENST00000551634.6:c.1847G>C	ENSP00000448373.2:p.Ser616Thr
ENST00000680362.1:c.1738G>C
ENST00000681323.1:c.793+2564G>C
ENST00000346562.6:c.1742G>C	ENSP00000319610.5:p.Ser581Thr
ENST00000356141.8:c.1838G>C	ENSP00000348460.4:p.Ser613Thr
ENST00000357798.9:c.1799G>C	ENSP00000350446.5:p.Ser600Thr
ENST00000548645.5:c.1748G>C	ENSP00000448916.1:p.Ser583Thr
ENST00000551492.5:c.1853G>C	ENSP00000450392.1:p.Ser618Thr
ENST00000551634.5:c.1760G>C	ENSP00000448373.1:p.Ser587Thr
NM_001164749.1:c.1838G>C	NP_001158221.1:p.Ser613Thr
NM_001165893.1:c.1748G>C	NP_001159365.1:p.Ser583Thr
NM_022123.2:c.1742G>C	NP_071406.1:p.Ser581Thr
NM_173159.2:c.1799G>C	NP_775182.1:p.Ser600Thr
XM_005267991.2:c.1859G>C	XP_005268048.1:p.Ser620Thr
XM_005267992.2:c.1853G>C	XP_005268049.1:p.Ser618Thr
XM_005267993.2:c.1799G>C	XP_005268050.1:p.Ser600Thr
XM_011537067.1:c.1889G>C	XP_011535369.1:p.Ser630Thr
XM_011537068.1:c.1880G>C	XP_011535370.1:p.Ser627Thr
XM_011537069.1:c.1850G>C	XP_011535371.1:p.Ser617Thr
XM_011537070.1:c.1793G>C	XP_011535372.1:p.Ser598Thr
XM_011537071.1:c.1760G>C	XP_011535373.1:p.Ser587Thr
XM_011537072.1:c.1739G>C	XP_011535374.1:p.Ser580Thr
XM_011537073.1:c.1532G>C	XP_011535375.1:p.Ser511Thr
XM_011537074.1:c.1532G>C	XP_011535376.1:p.Ser511Thr
XM_005267991.3:c.1946G>C	XP_005268048.2:p.Ser649Thr
XM_005267992.3:c.1940G>C	XP_005268049.2:p.Ser647Thr
XM_011537067.2:c.1889G>C	XP_011535369.1:p.Ser630Thr
XM_011537069.2:c.1937G>C	XP_011535371.2:p.Ser646Thr
XM_011537070.2:c.1793G>C	XP_011535372.1:p.Ser598Thr
XM_011537071.2:c.1847G>C	XP_011535373.2:p.Ser616Thr
XM_011537072.2:c.1739G>C	XP_011535374.1:p.Ser580Thr
XM_017021582.1:c.1997G>C	XP_016877071.1:p.Ser666Thr
XM_017021583.1:c.1988G>C	XP_016877072.1:p.Ser663Thr
XM_017021584.1:c.1907G>C	XP_016877073.1:p.Ser636Thr
XM_017021585.1:c.1856G>C	XP_016877074.1:p.Ser619Thr
XM_017021586.1:c.1532G>C	XP_016877075.1:p.Ser511Thr
XM_017021587.1:c.1532G>C	XP_016877076.1:p.Ser511Thr
XM_017021588.1:c.1532G>C	XP_016877077.1:p.Ser511Thr
NM_001164749.2:c.1838G>C MANE Select	NP_001158221.1:p.Ser613Thr
NM_001165893.2:c.1748G>C	NP_001159365.1:p.Ser583Thr
NM_022123.3:c.1742G>C	NP_071406.1:p.Ser581Thr
NM_173159.3:c.1799G>C	NP_775182.1:p.Ser600Thr
NM_001394988.1:c.1793G>C	NP_001381917.1:p.Ser598Thr
NM_001394989.1:c.1739G>C	NP_001381918.1:p.Ser580Thr