Canonical Allele Identifier: CA389412316

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269285C>A (hg19) ; chr14:g.33800079C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800079C>A , CM000676.2:g.33800079C>A	GRCh38
NC_000014.8:g.34269285C>A , CM000676.1:g.34269285C>A	GRCh37
NC_000014.7:g.33339036C>A	NCBI36
NG_013036.1:g.865827C>A
NG_013036.2:g.865827C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1772C>A MANE Select	ENSP00000348460.4:p.Ala591Glu
ENST00000551634.6:c.1781C>A	ENSP00000448373.2:p.Ala594Glu
ENST00000680362.1:c.1672C>A
ENST00000681323.1:c.793+2498C>A
ENST00000346562.6:c.1676C>A	ENSP00000319610.5:p.Ala559Glu
ENST00000356141.8:c.1772C>A	ENSP00000348460.4:p.Ala591Glu
ENST00000357798.9:c.1733C>A	ENSP00000350446.5:p.Ala578Glu
ENST00000548645.5:c.1682C>A	ENSP00000448916.1:p.Ala561Glu
ENST00000551492.5:c.1787C>A	ENSP00000450392.1:p.Ala596Glu
ENST00000551634.5:c.1694C>A	ENSP00000448373.1:p.Ala565Glu
NM_001164749.1:c.1772C>A	NP_001158221.1:p.Ala591Glu
NM_001165893.1:c.1682C>A	NP_001159365.1:p.Ala561Glu
NM_022123.2:c.1676C>A	NP_071406.1:p.Ala559Glu
NM_173159.2:c.1733C>A	NP_775182.1:p.Ala578Glu
XM_005267991.2:c.1793C>A	XP_005268048.1:p.Ala598Glu
XM_005267992.2:c.1787C>A	XP_005268049.1:p.Ala596Glu
XM_005267993.2:c.1733C>A	XP_005268050.1:p.Ala578Glu
XM_011537067.1:c.1823C>A	XP_011535369.1:p.Ala608Glu
XM_011537068.1:c.1814C>A	XP_011535370.1:p.Ala605Glu
XM_011537069.1:c.1784C>A	XP_011535371.1:p.Ala595Glu
XM_011537070.1:c.1727C>A	XP_011535372.1:p.Ala576Glu
XM_011537071.1:c.1694C>A	XP_011535373.1:p.Ala565Glu
XM_011537072.1:c.1673C>A	XP_011535374.1:p.Ala558Glu
XM_011537073.1:c.1466C>A	XP_011535375.1:p.Ala489Glu
XM_011537074.1:c.1466C>A	XP_011535376.1:p.Ala489Glu
XM_005267991.3:c.1880C>A	XP_005268048.2:p.Ala627Glu
XM_005267992.3:c.1874C>A	XP_005268049.2:p.Ala625Glu
XM_011537067.2:c.1823C>A	XP_011535369.1:p.Ala608Glu
XM_011537069.2:c.1871C>A	XP_011535371.2:p.Ala624Glu
XM_011537070.2:c.1727C>A	XP_011535372.1:p.Ala576Glu
XM_011537071.2:c.1781C>A	XP_011535373.2:p.Ala594Glu
XM_011537072.2:c.1673C>A	XP_011535374.1:p.Ala558Glu
XM_017021582.1:c.1931C>A	XP_016877071.1:p.Ala644Glu
XM_017021583.1:c.1922C>A	XP_016877072.1:p.Ala641Glu
XM_017021584.1:c.1841C>A	XP_016877073.1:p.Ala614Glu
XM_017021585.1:c.1790C>A	XP_016877074.1:p.Ala597Glu
XM_017021586.1:c.1466C>A	XP_016877075.1:p.Ala489Glu
XM_017021587.1:c.1466C>A	XP_016877076.1:p.Ala489Glu
XM_017021588.1:c.1466C>A	XP_016877077.1:p.Ala489Glu
NM_001164749.2:c.1772C>A MANE Select	NP_001158221.1:p.Ala591Glu
NM_001165893.2:c.1682C>A	NP_001159365.1:p.Ala561Glu
NM_022123.3:c.1676C>A	NP_071406.1:p.Ala559Glu
NM_173159.3:c.1733C>A	NP_775182.1:p.Ala578Glu
NM_001394988.1:c.1727C>A	NP_001381917.1:p.Ala576Glu
NM_001394989.1:c.1673C>A	NP_001381918.1:p.Ala558Glu