Canonical Allele Identifier: CA389412202

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269267G>C (hg19) ; chr14:g.33800061G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800061G>C , CM000676.2:g.33800061G>C	GRCh38
NC_000014.8:g.34269267G>C , CM000676.1:g.34269267G>C	GRCh37
NC_000014.7:g.33339018G>C	NCBI36
NG_013036.1:g.865809G>C
NG_013036.2:g.865809G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1754G>C MANE Select	ENSP00000348460.4:p.Ser585Thr
ENST00000551634.6:c.1763G>C	ENSP00000448373.2:p.Ser588Thr
ENST00000680362.1:c.1654G>C
ENST00000681323.1:c.793+2480G>C
ENST00000346562.6:c.1658G>C	ENSP00000319610.5:p.Ser553Thr
ENST00000356141.8:c.1754G>C	ENSP00000348460.4:p.Ser585Thr
ENST00000357798.9:c.1715G>C	ENSP00000350446.5:p.Ser572Thr
ENST00000548645.5:c.1664G>C	ENSP00000448916.1:p.Ser555Thr
ENST00000551492.5:c.1769G>C	ENSP00000450392.1:p.Ser590Thr
ENST00000551634.5:c.1676G>C	ENSP00000448373.1:p.Ser559Thr
NM_001164749.1:c.1754G>C	NP_001158221.1:p.Ser585Thr
NM_001165893.1:c.1664G>C	NP_001159365.1:p.Ser555Thr
NM_022123.2:c.1658G>C	NP_071406.1:p.Ser553Thr
NM_173159.2:c.1715G>C	NP_775182.1:p.Ser572Thr
XM_005267991.2:c.1775G>C	XP_005268048.1:p.Ser592Thr
XM_005267992.2:c.1769G>C	XP_005268049.1:p.Ser590Thr
XM_005267993.2:c.1715G>C	XP_005268050.1:p.Ser572Thr
XM_011537067.1:c.1805G>C	XP_011535369.1:p.Ser602Thr
XM_011537068.1:c.1796G>C	XP_011535370.1:p.Ser599Thr
XM_011537069.1:c.1766G>C	XP_011535371.1:p.Ser589Thr
XM_011537070.1:c.1709G>C	XP_011535372.1:p.Ser570Thr
XM_011537071.1:c.1676G>C	XP_011535373.1:p.Ser559Thr
XM_011537072.1:c.1655G>C	XP_011535374.1:p.Ser552Thr
XM_011537073.1:c.1448G>C	XP_011535375.1:p.Ser483Thr
XM_011537074.1:c.1448G>C	XP_011535376.1:p.Ser483Thr
XM_005267991.3:c.1862G>C	XP_005268048.2:p.Ser621Thr
XM_005267992.3:c.1856G>C	XP_005268049.2:p.Ser619Thr
XM_011537067.2:c.1805G>C	XP_011535369.1:p.Ser602Thr
XM_011537069.2:c.1853G>C	XP_011535371.2:p.Ser618Thr
XM_011537070.2:c.1709G>C	XP_011535372.1:p.Ser570Thr
XM_011537071.2:c.1763G>C	XP_011535373.2:p.Ser588Thr
XM_011537072.2:c.1655G>C	XP_011535374.1:p.Ser552Thr
XM_017021582.1:c.1913G>C	XP_016877071.1:p.Ser638Thr
XM_017021583.1:c.1904G>C	XP_016877072.1:p.Ser635Thr
XM_017021584.1:c.1823G>C	XP_016877073.1:p.Ser608Thr
XM_017021585.1:c.1772G>C	XP_016877074.1:p.Ser591Thr
XM_017021586.1:c.1448G>C	XP_016877075.1:p.Ser483Thr
XM_017021587.1:c.1448G>C	XP_016877076.1:p.Ser483Thr
XM_017021588.1:c.1448G>C	XP_016877077.1:p.Ser483Thr
NM_001164749.2:c.1754G>C MANE Select	NP_001158221.1:p.Ser585Thr
NM_001165893.2:c.1664G>C	NP_001159365.1:p.Ser555Thr
NM_022123.3:c.1658G>C	NP_071406.1:p.Ser553Thr
NM_173159.3:c.1715G>C	NP_775182.1:p.Ser572Thr
NM_001394988.1:c.1709G>C	NP_001381917.1:p.Ser570Thr
NM_001394989.1:c.1655G>C	NP_001381918.1:p.Ser552Thr