Canonical Allele Identifier: CA389412231

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269273G>A (hg19) ; chr14:g.33800067G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800067G>A , CM000676.2:g.33800067G>A	GRCh38
NC_000014.8:g.34269273G>A , CM000676.1:g.34269273G>A	GRCh37
NC_000014.7:g.33339024G>A	NCBI36
NG_013036.1:g.865815G>A
NG_013036.2:g.865815G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1760G>A MANE Select	ENSP00000348460.4:p.Gly587Asp
ENST00000551634.6:c.1769G>A	ENSP00000448373.2:p.Gly590Asp
ENST00000680362.1:c.1660G>A
ENST00000681323.1:c.793+2486G>A
ENST00000346562.6:c.1664G>A	ENSP00000319610.5:p.Gly555Asp
ENST00000356141.8:c.1760G>A	ENSP00000348460.4:p.Gly587Asp
ENST00000357798.9:c.1721G>A	ENSP00000350446.5:p.Gly574Asp
ENST00000548645.5:c.1670G>A	ENSP00000448916.1:p.Gly557Asp
ENST00000551492.5:c.1775G>A	ENSP00000450392.1:p.Gly592Asp
ENST00000551634.5:c.1682G>A	ENSP00000448373.1:p.Gly561Asp
NM_001164749.1:c.1760G>A	NP_001158221.1:p.Gly587Asp
NM_001165893.1:c.1670G>A	NP_001159365.1:p.Gly557Asp
NM_022123.2:c.1664G>A	NP_071406.1:p.Gly555Asp
NM_173159.2:c.1721G>A	NP_775182.1:p.Gly574Asp
XM_005267991.2:c.1781G>A	XP_005268048.1:p.Gly594Asp
XM_005267992.2:c.1775G>A	XP_005268049.1:p.Gly592Asp
XM_005267993.2:c.1721G>A	XP_005268050.1:p.Gly574Asp
XM_011537067.1:c.1811G>A	XP_011535369.1:p.Gly604Asp
XM_011537068.1:c.1802G>A	XP_011535370.1:p.Gly601Asp
XM_011537069.1:c.1772G>A	XP_011535371.1:p.Gly591Asp
XM_011537070.1:c.1715G>A	XP_011535372.1:p.Gly572Asp
XM_011537071.1:c.1682G>A	XP_011535373.1:p.Gly561Asp
XM_011537072.1:c.1661G>A	XP_011535374.1:p.Gly554Asp
XM_011537073.1:c.1454G>A	XP_011535375.1:p.Gly485Asp
XM_011537074.1:c.1454G>A	XP_011535376.1:p.Gly485Asp
XM_005267991.3:c.1868G>A	XP_005268048.2:p.Gly623Asp
XM_005267992.3:c.1862G>A	XP_005268049.2:p.Gly621Asp
XM_011537067.2:c.1811G>A	XP_011535369.1:p.Gly604Asp
XM_011537069.2:c.1859G>A	XP_011535371.2:p.Gly620Asp
XM_011537070.2:c.1715G>A	XP_011535372.1:p.Gly572Asp
XM_011537071.2:c.1769G>A	XP_011535373.2:p.Gly590Asp
XM_011537072.2:c.1661G>A	XP_011535374.1:p.Gly554Asp
XM_017021582.1:c.1919G>A	XP_016877071.1:p.Gly640Asp
XM_017021583.1:c.1910G>A	XP_016877072.1:p.Gly637Asp
XM_017021584.1:c.1829G>A	XP_016877073.1:p.Gly610Asp
XM_017021585.1:c.1778G>A	XP_016877074.1:p.Gly593Asp
XM_017021586.1:c.1454G>A	XP_016877075.1:p.Gly485Asp
XM_017021587.1:c.1454G>A	XP_016877076.1:p.Gly485Asp
XM_017021588.1:c.1454G>A	XP_016877077.1:p.Gly485Asp
NM_001164749.2:c.1760G>A MANE Select	NP_001158221.1:p.Gly587Asp
NM_001165893.2:c.1670G>A	NP_001159365.1:p.Gly557Asp
NM_022123.3:c.1664G>A	NP_071406.1:p.Gly555Asp
NM_173159.3:c.1721G>A	NP_775182.1:p.Gly574Asp
NM_001394988.1:c.1715G>A	NP_001381917.1:p.Gly572Asp
NM_001394989.1:c.1661G>A	NP_001381918.1:p.Gly554Asp