Canonical Allele Identifier: CA389414161

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269699C>G (hg19) ; chr14:g.33800493C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800493C>G , CM000676.2:g.33800493C>G	GRCh38
NC_000014.8:g.34269699C>G , CM000676.1:g.34269699C>G	GRCh37
NC_000014.7:g.33339450C>G	NCBI36
NG_013036.1:g.866241C>G
NG_013036.2:g.866241C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2186C>G MANE Select	ENSP00000348460.4:p.Thr729Ser
ENST00000551634.6:c.2195C>G	ENSP00000448373.2:p.Thr732Ser
ENST00000680362.1:c.2086C>G
ENST00000681323.1:c.793+2912C>G
ENST00000346562.6:c.2090C>G	ENSP00000319610.5:p.Thr697Ser
ENST00000356141.8:c.2186C>G	ENSP00000348460.4:p.Thr729Ser
ENST00000357798.9:c.2147C>G	ENSP00000350446.5:p.Thr716Ser
ENST00000548645.5:c.2096C>G	ENSP00000448916.1:p.Thr699Ser
ENST00000551492.5:c.2201C>G	ENSP00000450392.1:p.Thr734Ser
ENST00000551634.5:c.2108C>G	ENSP00000448373.1:p.Thr703Ser
NM_001164749.1:c.2186C>G	NP_001158221.1:p.Thr729Ser
NM_001165893.1:c.2096C>G	NP_001159365.1:p.Thr699Ser
NM_022123.2:c.2090C>G	NP_071406.1:p.Thr697Ser
NM_173159.2:c.2147C>G	NP_775182.1:p.Thr716Ser
XM_005267991.2:c.2207C>G	XP_005268048.1:p.Thr736Ser
XM_005267992.2:c.2201C>G	XP_005268049.1:p.Thr734Ser
XM_005267993.2:c.2147C>G	XP_005268050.1:p.Thr716Ser
XM_011537067.1:c.2237C>G	XP_011535369.1:p.Thr746Ser
XM_011537068.1:c.2228C>G	XP_011535370.1:p.Thr743Ser
XM_011537069.1:c.2198C>G	XP_011535371.1:p.Thr733Ser
XM_011537070.1:c.2141C>G	XP_011535372.1:p.Thr714Ser
XM_011537071.1:c.2108C>G	XP_011535373.1:p.Thr703Ser
XM_011537072.1:c.2087C>G	XP_011535374.1:p.Thr696Ser
XM_011537073.1:c.1880C>G	XP_011535375.1:p.Thr627Ser
XM_011537074.1:c.1880C>G	XP_011535376.1:p.Thr627Ser
XM_005267991.3:c.2294C>G	XP_005268048.2:p.Thr765Ser
XM_005267992.3:c.2288C>G	XP_005268049.2:p.Thr763Ser
XM_011537067.2:c.2237C>G	XP_011535369.1:p.Thr746Ser
XM_011537069.2:c.2285C>G	XP_011535371.2:p.Thr762Ser
XM_011537070.2:c.2141C>G	XP_011535372.1:p.Thr714Ser
XM_011537071.2:c.2195C>G	XP_011535373.2:p.Thr732Ser
XM_011537072.2:c.2087C>G	XP_011535374.1:p.Thr696Ser
XM_017021582.1:c.2345C>G	XP_016877071.1:p.Thr782Ser
XM_017021583.1:c.2336C>G	XP_016877072.1:p.Thr779Ser
XM_017021584.1:c.2255C>G	XP_016877073.1:p.Thr752Ser
XM_017021585.1:c.2204C>G	XP_016877074.1:p.Thr735Ser
XM_017021586.1:c.1880C>G	XP_016877075.1:p.Thr627Ser
XM_017021587.1:c.1880C>G	XP_016877076.1:p.Thr627Ser
XM_017021588.1:c.1880C>G	XP_016877077.1:p.Thr627Ser
NM_001164749.2:c.2186C>G MANE Select	NP_001158221.1:p.Thr729Ser
NM_001165893.2:c.2096C>G	NP_001159365.1:p.Thr699Ser
NM_022123.3:c.2090C>G	NP_071406.1:p.Thr697Ser
NM_173159.3:c.2147C>G	NP_775182.1:p.Thr716Ser
NM_001394988.1:c.2141C>G	NP_001381917.1:p.Thr714Ser
NM_001394989.1:c.2087C>G	NP_001381918.1:p.Thr696Ser