Canonical Allele Identifier: CA486092814

Gene: NPAS3

Linked Data

• dbSNP Id: rs755274978
• MyVariant Identifiers: chr14:g.34269340C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800134C>A , CM000676.2:g.33800134C>A	GRCh38
NC_000014.8:g.34269340C>A , CM000676.1:g.34269340C>A	GRCh37
NC_000014.7:g.33339091C>A	NCBI36
NG_013036.1:g.865882C>A
NG_013036.2:g.865882C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1827C>A MANE Select	ENSP00000348460.4:p.Gly609=
ENST00000551634.6:c.1836C>A	ENSP00000448373.2:p.Gly612=
ENST00000680362.1:c.1727C>A
ENST00000681323.1:c.793+2553C>A
ENST00000346562.6:c.1731C>A	ENSP00000319610.5:p.Gly577=
ENST00000356141.8:c.1827C>A	ENSP00000348460.4:p.Gly609=
ENST00000357798.9:c.1788C>A	ENSP00000350446.5:p.Gly596=
ENST00000548645.5:c.1737C>A	ENSP00000448916.1:p.Gly579=
ENST00000551492.5:c.1842C>A	ENSP00000450392.1:p.Gly614=
ENST00000551634.5:c.1749C>A	ENSP00000448373.1:p.Gly583=
NM_001164749.1:c.1827C>A	NP_001158221.1:p.Gly609=
NM_001165893.1:c.1737C>A	NP_001159365.1:p.Gly579=
NM_022123.2:c.1731C>A	NP_071406.1:p.Gly577=
NM_173159.2:c.1788C>A	NP_775182.1:p.Gly596=
XM_005267991.2:c.1848C>A	XP_005268048.1:p.Gly616=
XM_005267992.2:c.1842C>A	XP_005268049.1:p.Gly614=
XM_005267993.2:c.1788C>A	XP_005268050.1:p.Gly596=
XM_011537067.1:c.1878C>A	XP_011535369.1:p.Gly626=
XM_011537068.1:c.1869C>A	XP_011535370.1:p.Gly623=
XM_011537069.1:c.1839C>A	XP_011535371.1:p.Gly613=
XM_011537070.1:c.1782C>A	XP_011535372.1:p.Gly594=
XM_011537071.1:c.1749C>A	XP_011535373.1:p.Gly583=
XM_011537072.1:c.1728C>A	XP_011535374.1:p.Gly576=
XM_011537073.1:c.1521C>A	XP_011535375.1:p.Gly507=
XM_011537074.1:c.1521C>A	XP_011535376.1:p.Gly507=
XM_005267991.3:c.1935C>A	XP_005268048.2:p.Gly645=
XM_005267992.3:c.1929C>A	XP_005268049.2:p.Gly643=
XM_011537067.2:c.1878C>A	XP_011535369.1:p.Gly626=
XM_011537069.2:c.1926C>A	XP_011535371.2:p.Gly642=
XM_011537070.2:c.1782C>A	XP_011535372.1:p.Gly594=
XM_011537071.2:c.1836C>A	XP_011535373.2:p.Gly612=
XM_011537072.2:c.1728C>A	XP_011535374.1:p.Gly576=
XM_017021582.1:c.1986C>A	XP_016877071.1:p.Gly662=
XM_017021583.1:c.1977C>A	XP_016877072.1:p.Gly659=
XM_017021584.1:c.1896C>A	XP_016877073.1:p.Gly632=
XM_017021585.1:c.1845C>A	XP_016877074.1:p.Gly615=
XM_017021586.1:c.1521C>A	XP_016877075.1:p.Gly507=
XM_017021587.1:c.1521C>A	XP_016877076.1:p.Gly507=
XM_017021588.1:c.1521C>A	XP_016877077.1:p.Gly507=
NM_001164749.2:c.1827C>A MANE Select	NP_001158221.1:p.Gly609=
NM_001165893.2:c.1737C>A	NP_001159365.1:p.Gly579=
NM_022123.3:c.1731C>A	NP_071406.1:p.Gly577=
NM_173159.3:c.1788C>A	NP_775182.1:p.Gly596=
NM_001394988.1:c.1782C>A	NP_001381917.1:p.Gly594=
NM_001394989.1:c.1728C>A	NP_001381918.1:p.Gly576=