Canonical Allele Identifier: CA486092863

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269382A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800176A>T , CM000676.2:g.33800176A>T	GRCh38
NC_000014.8:g.34269382A>T , CM000676.1:g.34269382A>T	GRCh37
NC_000014.7:g.33339133A>T	NCBI36
NG_013036.1:g.865924A>T
NG_013036.2:g.865924A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1869A>T MANE Select	ENSP00000348460.4:p.Pro623=
ENST00000551634.6:c.1878A>T	ENSP00000448373.2:p.Pro626=
ENST00000680362.1:c.1769A>T
ENST00000681323.1:c.793+2595A>T
ENST00000346562.6:c.1773A>T	ENSP00000319610.5:p.Pro591=
ENST00000356141.8:c.1869A>T	ENSP00000348460.4:p.Pro623=
ENST00000357798.9:c.1830A>T	ENSP00000350446.5:p.Pro610=
ENST00000548645.5:c.1779A>T	ENSP00000448916.1:p.Pro593=
ENST00000551492.5:c.1884A>T	ENSP00000450392.1:p.Pro628=
ENST00000551634.5:c.1791A>T	ENSP00000448373.1:p.Pro597=
NM_001164749.1:c.1869A>T	NP_001158221.1:p.Pro623=
NM_001165893.1:c.1779A>T	NP_001159365.1:p.Pro593=
NM_022123.2:c.1773A>T	NP_071406.1:p.Pro591=
NM_173159.2:c.1830A>T	NP_775182.1:p.Pro610=
XM_005267991.2:c.1890A>T	XP_005268048.1:p.Pro630=
XM_005267992.2:c.1884A>T	XP_005268049.1:p.Pro628=
XM_005267993.2:c.1830A>T	XP_005268050.1:p.Pro610=
XM_011537067.1:c.1920A>T	XP_011535369.1:p.Pro640=
XM_011537068.1:c.1911A>T	XP_011535370.1:p.Pro637=
XM_011537069.1:c.1881A>T	XP_011535371.1:p.Pro627=
XM_011537070.1:c.1824A>T	XP_011535372.1:p.Pro608=
XM_011537071.1:c.1791A>T	XP_011535373.1:p.Pro597=
XM_011537072.1:c.1770A>T	XP_011535374.1:p.Pro590=
XM_011537073.1:c.1563A>T	XP_011535375.1:p.Pro521=
XM_011537074.1:c.1563A>T	XP_011535376.1:p.Pro521=
XM_005267991.3:c.1977A>T	XP_005268048.2:p.Pro659=
XM_005267992.3:c.1971A>T	XP_005268049.2:p.Pro657=
XM_011537067.2:c.1920A>T	XP_011535369.1:p.Pro640=
XM_011537069.2:c.1968A>T	XP_011535371.2:p.Pro656=
XM_011537070.2:c.1824A>T	XP_011535372.1:p.Pro608=
XM_011537071.2:c.1878A>T	XP_011535373.2:p.Pro626=
XM_011537072.2:c.1770A>T	XP_011535374.1:p.Pro590=
XM_017021582.1:c.2028A>T	XP_016877071.1:p.Pro676=
XM_017021583.1:c.2019A>T	XP_016877072.1:p.Pro673=
XM_017021584.1:c.1938A>T	XP_016877073.1:p.Pro646=
XM_017021585.1:c.1887A>T	XP_016877074.1:p.Pro629=
XM_017021586.1:c.1563A>T	XP_016877075.1:p.Pro521=
XM_017021587.1:c.1563A>T	XP_016877076.1:p.Pro521=
XM_017021588.1:c.1563A>T	XP_016877077.1:p.Pro521=
NM_001164749.2:c.1869A>T MANE Select	NP_001158221.1:p.Pro623=
NM_001165893.2:c.1779A>T	NP_001159365.1:p.Pro593=
NM_022123.3:c.1773A>T	NP_071406.1:p.Pro591=
NM_173159.3:c.1830A>T	NP_775182.1:p.Pro610=
NM_001394988.1:c.1824A>T	NP_001381917.1:p.Pro608=
NM_001394989.1:c.1770A>T	NP_001381918.1:p.Pro590=