Canonical Allele Identifier: CA389412370

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269297G>C (hg19) ; chr14:g.33800091G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800091G>C , CM000676.2:g.33800091G>C	GRCh38
NC_000014.8:g.34269297G>C , CM000676.1:g.34269297G>C	GRCh37
NC_000014.7:g.33339048G>C	NCBI36
NG_013036.1:g.865839G>C
NG_013036.2:g.865839G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1784G>C MANE Select	ENSP00000348460.4:p.Ser595Thr
ENST00000551634.6:c.1793G>C	ENSP00000448373.2:p.Ser598Thr
ENST00000680362.1:c.1684G>C
ENST00000681323.1:c.793+2510G>C
ENST00000346562.6:c.1688G>C	ENSP00000319610.5:p.Ser563Thr
ENST00000356141.8:c.1784G>C	ENSP00000348460.4:p.Ser595Thr
ENST00000357798.9:c.1745G>C	ENSP00000350446.5:p.Ser582Thr
ENST00000548645.5:c.1694G>C	ENSP00000448916.1:p.Ser565Thr
ENST00000551492.5:c.1799G>C	ENSP00000450392.1:p.Ser600Thr
ENST00000551634.5:c.1706G>C	ENSP00000448373.1:p.Ser569Thr
NM_001164749.1:c.1784G>C	NP_001158221.1:p.Ser595Thr
NM_001165893.1:c.1694G>C	NP_001159365.1:p.Ser565Thr
NM_022123.2:c.1688G>C	NP_071406.1:p.Ser563Thr
NM_173159.2:c.1745G>C	NP_775182.1:p.Ser582Thr
XM_005267991.2:c.1805G>C	XP_005268048.1:p.Ser602Thr
XM_005267992.2:c.1799G>C	XP_005268049.1:p.Ser600Thr
XM_005267993.2:c.1745G>C	XP_005268050.1:p.Ser582Thr
XM_011537067.1:c.1835G>C	XP_011535369.1:p.Ser612Thr
XM_011537068.1:c.1826G>C	XP_011535370.1:p.Ser609Thr
XM_011537069.1:c.1796G>C	XP_011535371.1:p.Ser599Thr
XM_011537070.1:c.1739G>C	XP_011535372.1:p.Ser580Thr
XM_011537071.1:c.1706G>C	XP_011535373.1:p.Ser569Thr
XM_011537072.1:c.1685G>C	XP_011535374.1:p.Ser562Thr
XM_011537073.1:c.1478G>C	XP_011535375.1:p.Ser493Thr
XM_011537074.1:c.1478G>C	XP_011535376.1:p.Ser493Thr
XM_005267991.3:c.1892G>C	XP_005268048.2:p.Ser631Thr
XM_005267992.3:c.1886G>C	XP_005268049.2:p.Ser629Thr
XM_011537067.2:c.1835G>C	XP_011535369.1:p.Ser612Thr
XM_011537069.2:c.1883G>C	XP_011535371.2:p.Ser628Thr
XM_011537070.2:c.1739G>C	XP_011535372.1:p.Ser580Thr
XM_011537071.2:c.1793G>C	XP_011535373.2:p.Ser598Thr
XM_011537072.2:c.1685G>C	XP_011535374.1:p.Ser562Thr
XM_017021582.1:c.1943G>C	XP_016877071.1:p.Ser648Thr
XM_017021583.1:c.1934G>C	XP_016877072.1:p.Ser645Thr
XM_017021584.1:c.1853G>C	XP_016877073.1:p.Ser618Thr
XM_017021585.1:c.1802G>C	XP_016877074.1:p.Ser601Thr
XM_017021586.1:c.1478G>C	XP_016877075.1:p.Ser493Thr
XM_017021587.1:c.1478G>C	XP_016877076.1:p.Ser493Thr
XM_017021588.1:c.1478G>C	XP_016877077.1:p.Ser493Thr
NM_001164749.2:c.1784G>C MANE Select	NP_001158221.1:p.Ser595Thr
NM_001165893.2:c.1694G>C	NP_001159365.1:p.Ser565Thr
NM_022123.3:c.1688G>C	NP_071406.1:p.Ser563Thr
NM_173159.3:c.1745G>C	NP_775182.1:p.Ser582Thr
NM_001394988.1:c.1739G>C	NP_001381917.1:p.Ser580Thr
NM_001394989.1:c.1685G>C	NP_001381918.1:p.Ser562Thr