Canonical Allele Identifier: CA389413682

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269560A>T (hg19) ; chr14:g.33800354A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800354A>T , CM000676.2:g.33800354A>T	GRCh38
NC_000014.8:g.34269560A>T , CM000676.1:g.34269560A>T	GRCh37
NC_000014.7:g.33339311A>T	NCBI36
NG_013036.1:g.866102A>T
NG_013036.2:g.866102A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2047A>T MANE Select	ENSP00000348460.4:p.Thr683Ser
ENST00000551634.6:c.2056A>T	ENSP00000448373.2:p.Thr686Ser
ENST00000680362.1:c.1947A>T
ENST00000681323.1:c.793+2773A>T
ENST00000346562.6:c.1951A>T	ENSP00000319610.5:p.Thr651Ser
ENST00000356141.8:c.2047A>T	ENSP00000348460.4:p.Thr683Ser
ENST00000357798.9:c.2008A>T	ENSP00000350446.5:p.Thr670Ser
ENST00000548645.5:c.1957A>T	ENSP00000448916.1:p.Thr653Ser
ENST00000551492.5:c.2062A>T	ENSP00000450392.1:p.Thr688Ser
ENST00000551634.5:c.1969A>T	ENSP00000448373.1:p.Thr657Ser
NM_001164749.1:c.2047A>T	NP_001158221.1:p.Thr683Ser
NM_001165893.1:c.1957A>T	NP_001159365.1:p.Thr653Ser
NM_022123.2:c.1951A>T	NP_071406.1:p.Thr651Ser
NM_173159.2:c.2008A>T	NP_775182.1:p.Thr670Ser
XM_005267991.2:c.2068A>T	XP_005268048.1:p.Thr690Ser
XM_005267992.2:c.2062A>T	XP_005268049.1:p.Thr688Ser
XM_005267993.2:c.2008A>T	XP_005268050.1:p.Thr670Ser
XM_011537067.1:c.2098A>T	XP_011535369.1:p.Thr700Ser
XM_011537068.1:c.2089A>T	XP_011535370.1:p.Thr697Ser
XM_011537069.1:c.2059A>T	XP_011535371.1:p.Thr687Ser
XM_011537070.1:c.2002A>T	XP_011535372.1:p.Thr668Ser
XM_011537071.1:c.1969A>T	XP_011535373.1:p.Thr657Ser
XM_011537072.1:c.1948A>T	XP_011535374.1:p.Thr650Ser
XM_011537073.1:c.1741A>T	XP_011535375.1:p.Thr581Ser
XM_011537074.1:c.1741A>T	XP_011535376.1:p.Thr581Ser
XM_005267991.3:c.2155A>T	XP_005268048.2:p.Thr719Ser
XM_005267992.3:c.2149A>T	XP_005268049.2:p.Thr717Ser
XM_011537067.2:c.2098A>T	XP_011535369.1:p.Thr700Ser
XM_011537069.2:c.2146A>T	XP_011535371.2:p.Thr716Ser
XM_011537070.2:c.2002A>T	XP_011535372.1:p.Thr668Ser
XM_011537071.2:c.2056A>T	XP_011535373.2:p.Thr686Ser
XM_011537072.2:c.1948A>T	XP_011535374.1:p.Thr650Ser
XM_017021582.1:c.2206A>T	XP_016877071.1:p.Thr736Ser
XM_017021583.1:c.2197A>T	XP_016877072.1:p.Thr733Ser
XM_017021584.1:c.2116A>T	XP_016877073.1:p.Thr706Ser
XM_017021585.1:c.2065A>T	XP_016877074.1:p.Thr689Ser
XM_017021586.1:c.1741A>T	XP_016877075.1:p.Thr581Ser
XM_017021587.1:c.1741A>T	XP_016877076.1:p.Thr581Ser
XM_017021588.1:c.1741A>T	XP_016877077.1:p.Thr581Ser
NM_001164749.2:c.2047A>T MANE Select	NP_001158221.1:p.Thr683Ser
NM_001165893.2:c.1957A>T	NP_001159365.1:p.Thr653Ser
NM_022123.3:c.1951A>T	NP_071406.1:p.Thr651Ser
NM_173159.3:c.2008A>T	NP_775182.1:p.Thr670Ser
NM_001394988.1:c.2002A>T	NP_001381917.1:p.Thr668Ser
NM_001394989.1:c.1948A>T	NP_001381918.1:p.Thr650Ser