Canonical Allele Identifier: CA389413145

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269443T>A (hg19) ; chr14:g.33800237T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800237T>A , CM000676.2:g.33800237T>A	GRCh38
NC_000014.8:g.34269443T>A , CM000676.1:g.34269443T>A	GRCh37
NC_000014.7:g.33339194T>A	NCBI36
NG_013036.1:g.865985T>A
NG_013036.2:g.865985T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1930T>A MANE Select	ENSP00000348460.4:p.Ser644Thr
ENST00000551634.6:c.1939T>A	ENSP00000448373.2:p.Ser647Thr
ENST00000680362.1:c.1830T>A
ENST00000681323.1:c.793+2656T>A
ENST00000346562.6:c.1834T>A	ENSP00000319610.5:p.Ser612Thr
ENST00000356141.8:c.1930T>A	ENSP00000348460.4:p.Ser644Thr
ENST00000357798.9:c.1891T>A	ENSP00000350446.5:p.Ser631Thr
ENST00000548645.5:c.1840T>A	ENSP00000448916.1:p.Ser614Thr
ENST00000551492.5:c.1945T>A	ENSP00000450392.1:p.Ser649Thr
ENST00000551634.5:c.1852T>A	ENSP00000448373.1:p.Ser618Thr
NM_001164749.1:c.1930T>A	NP_001158221.1:p.Ser644Thr
NM_001165893.1:c.1840T>A	NP_001159365.1:p.Ser614Thr
NM_022123.2:c.1834T>A	NP_071406.1:p.Ser612Thr
NM_173159.2:c.1891T>A	NP_775182.1:p.Ser631Thr
XM_005267991.2:c.1951T>A	XP_005268048.1:p.Ser651Thr
XM_005267992.2:c.1945T>A	XP_005268049.1:p.Ser649Thr
XM_005267993.2:c.1891T>A	XP_005268050.1:p.Ser631Thr
XM_011537067.1:c.1981T>A	XP_011535369.1:p.Ser661Thr
XM_011537068.1:c.1972T>A	XP_011535370.1:p.Ser658Thr
XM_011537069.1:c.1942T>A	XP_011535371.1:p.Ser648Thr
XM_011537070.1:c.1885T>A	XP_011535372.1:p.Ser629Thr
XM_011537071.1:c.1852T>A	XP_011535373.1:p.Ser618Thr
XM_011537072.1:c.1831T>A	XP_011535374.1:p.Ser611Thr
XM_011537073.1:c.1624T>A	XP_011535375.1:p.Ser542Thr
XM_011537074.1:c.1624T>A	XP_011535376.1:p.Ser542Thr
XM_005267991.3:c.2038T>A	XP_005268048.2:p.Ser680Thr
XM_005267992.3:c.2032T>A	XP_005268049.2:p.Ser678Thr
XM_011537067.2:c.1981T>A	XP_011535369.1:p.Ser661Thr
XM_011537069.2:c.2029T>A	XP_011535371.2:p.Ser677Thr
XM_011537070.2:c.1885T>A	XP_011535372.1:p.Ser629Thr
XM_011537071.2:c.1939T>A	XP_011535373.2:p.Ser647Thr
XM_011537072.2:c.1831T>A	XP_011535374.1:p.Ser611Thr
XM_017021582.1:c.2089T>A	XP_016877071.1:p.Ser697Thr
XM_017021583.1:c.2080T>A	XP_016877072.1:p.Ser694Thr
XM_017021584.1:c.1999T>A	XP_016877073.1:p.Ser667Thr
XM_017021585.1:c.1948T>A	XP_016877074.1:p.Ser650Thr
XM_017021586.1:c.1624T>A	XP_016877075.1:p.Ser542Thr
XM_017021587.1:c.1624T>A	XP_016877076.1:p.Ser542Thr
XM_017021588.1:c.1624T>A	XP_016877077.1:p.Ser542Thr
NM_001164749.2:c.1930T>A MANE Select	NP_001158221.1:p.Ser644Thr
NM_001165893.2:c.1840T>A	NP_001159365.1:p.Ser614Thr
NM_022123.3:c.1834T>A	NP_071406.1:p.Ser612Thr
NM_173159.3:c.1891T>A	NP_775182.1:p.Ser631Thr
NM_001394988.1:c.1885T>A	NP_001381917.1:p.Ser629Thr
NM_001394989.1:c.1831T>A	NP_001381918.1:p.Ser611Thr