Canonical Allele Identifier: CA389413225

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269462C>G (hg19) ; chr14:g.33800256C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800256C>G , CM000676.2:g.33800256C>G	GRCh38
NC_000014.8:g.34269462C>G , CM000676.1:g.34269462C>G	GRCh37
NC_000014.7:g.33339213C>G	NCBI36
NG_013036.1:g.866004C>G
NG_013036.2:g.866004C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1949C>G MANE Select	ENSP00000348460.4:p.Thr650Arg
ENST00000551634.6:c.1958C>G	ENSP00000448373.2:p.Thr653Arg
ENST00000680362.1:c.1849C>G
ENST00000681323.1:c.793+2675C>G
ENST00000346562.6:c.1853C>G	ENSP00000319610.5:p.Thr618Arg
ENST00000356141.8:c.1949C>G	ENSP00000348460.4:p.Thr650Arg
ENST00000357798.9:c.1910C>G	ENSP00000350446.5:p.Thr637Arg
ENST00000548645.5:c.1859C>G	ENSP00000448916.1:p.Thr620Arg
ENST00000551492.5:c.1964C>G	ENSP00000450392.1:p.Thr655Arg
ENST00000551634.5:c.1871C>G	ENSP00000448373.1:p.Thr624Arg
NM_001164749.1:c.1949C>G	NP_001158221.1:p.Thr650Arg
NM_001165893.1:c.1859C>G	NP_001159365.1:p.Thr620Arg
NM_022123.2:c.1853C>G	NP_071406.1:p.Thr618Arg
NM_173159.2:c.1910C>G	NP_775182.1:p.Thr637Arg
XM_005267991.2:c.1970C>G	XP_005268048.1:p.Thr657Arg
XM_005267992.2:c.1964C>G	XP_005268049.1:p.Thr655Arg
XM_005267993.2:c.1910C>G	XP_005268050.1:p.Thr637Arg
XM_011537067.1:c.2000C>G	XP_011535369.1:p.Thr667Arg
XM_011537068.1:c.1991C>G	XP_011535370.1:p.Thr664Arg
XM_011537069.1:c.1961C>G	XP_011535371.1:p.Thr654Arg
XM_011537070.1:c.1904C>G	XP_011535372.1:p.Thr635Arg
XM_011537071.1:c.1871C>G	XP_011535373.1:p.Thr624Arg
XM_011537072.1:c.1850C>G	XP_011535374.1:p.Thr617Arg
XM_011537073.1:c.1643C>G	XP_011535375.1:p.Thr548Arg
XM_011537074.1:c.1643C>G	XP_011535376.1:p.Thr548Arg
XM_005267991.3:c.2057C>G	XP_005268048.2:p.Thr686Arg
XM_005267992.3:c.2051C>G	XP_005268049.2:p.Thr684Arg
XM_011537067.2:c.2000C>G	XP_011535369.1:p.Thr667Arg
XM_011537069.2:c.2048C>G	XP_011535371.2:p.Thr683Arg
XM_011537070.2:c.1904C>G	XP_011535372.1:p.Thr635Arg
XM_011537071.2:c.1958C>G	XP_011535373.2:p.Thr653Arg
XM_011537072.2:c.1850C>G	XP_011535374.1:p.Thr617Arg
XM_017021582.1:c.2108C>G	XP_016877071.1:p.Thr703Arg
XM_017021583.1:c.2099C>G	XP_016877072.1:p.Thr700Arg
XM_017021584.1:c.2018C>G	XP_016877073.1:p.Thr673Arg
XM_017021585.1:c.1967C>G	XP_016877074.1:p.Thr656Arg
XM_017021586.1:c.1643C>G	XP_016877075.1:p.Thr548Arg
XM_017021587.1:c.1643C>G	XP_016877076.1:p.Thr548Arg
XM_017021588.1:c.1643C>G	XP_016877077.1:p.Thr548Arg
NM_001164749.2:c.1949C>G MANE Select	NP_001158221.1:p.Thr650Arg
NM_001165893.2:c.1859C>G	NP_001159365.1:p.Thr620Arg
NM_022123.3:c.1853C>G	NP_071406.1:p.Thr618Arg
NM_173159.3:c.1910C>G	NP_775182.1:p.Thr637Arg
NM_001394988.1:c.1904C>G	NP_001381917.1:p.Thr635Arg
NM_001394989.1:c.1850C>G	NP_001381918.1:p.Thr617Arg