Canonical Allele Identifier: CA389412968

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269398G>A (hg19) ; chr14:g.33800192G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800192G>A , CM000676.2:g.33800192G>A	GRCh38
NC_000014.8:g.34269398G>A , CM000676.1:g.34269398G>A	GRCh37
NC_000014.7:g.33339149G>A	NCBI36
NG_013036.1:g.865940G>A
NG_013036.2:g.865940G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1885G>A MANE Select	ENSP00000348460.4:p.Gly629Ser
ENST00000551634.6:c.1894G>A	ENSP00000448373.2:p.Gly632Ser
ENST00000680362.1:c.1785G>A
ENST00000681323.1:c.793+2611G>A
ENST00000346562.6:c.1789G>A	ENSP00000319610.5:p.Gly597Ser
ENST00000356141.8:c.1885G>A	ENSP00000348460.4:p.Gly629Ser
ENST00000357798.9:c.1846G>A	ENSP00000350446.5:p.Gly616Ser
ENST00000548645.5:c.1795G>A	ENSP00000448916.1:p.Gly599Ser
ENST00000551492.5:c.1900G>A	ENSP00000450392.1:p.Gly634Ser
ENST00000551634.5:c.1807G>A	ENSP00000448373.1:p.Gly603Ser
NM_001164749.1:c.1885G>A	NP_001158221.1:p.Gly629Ser
NM_001165893.1:c.1795G>A	NP_001159365.1:p.Gly599Ser
NM_022123.2:c.1789G>A	NP_071406.1:p.Gly597Ser
NM_173159.2:c.1846G>A	NP_775182.1:p.Gly616Ser
XM_005267991.2:c.1906G>A	XP_005268048.1:p.Gly636Ser
XM_005267992.2:c.1900G>A	XP_005268049.1:p.Gly634Ser
XM_005267993.2:c.1846G>A	XP_005268050.1:p.Gly616Ser
XM_011537067.1:c.1936G>A	XP_011535369.1:p.Gly646Ser
XM_011537068.1:c.1927G>A	XP_011535370.1:p.Gly643Ser
XM_011537069.1:c.1897G>A	XP_011535371.1:p.Gly633Ser
XM_011537070.1:c.1840G>A	XP_011535372.1:p.Gly614Ser
XM_011537071.1:c.1807G>A	XP_011535373.1:p.Gly603Ser
XM_011537072.1:c.1786G>A	XP_011535374.1:p.Gly596Ser
XM_011537073.1:c.1579G>A	XP_011535375.1:p.Gly527Ser
XM_011537074.1:c.1579G>A	XP_011535376.1:p.Gly527Ser
XM_005267991.3:c.1993G>A	XP_005268048.2:p.Gly665Ser
XM_005267992.3:c.1987G>A	XP_005268049.2:p.Gly663Ser
XM_011537067.2:c.1936G>A	XP_011535369.1:p.Gly646Ser
XM_011537069.2:c.1984G>A	XP_011535371.2:p.Gly662Ser
XM_011537070.2:c.1840G>A	XP_011535372.1:p.Gly614Ser
XM_011537071.2:c.1894G>A	XP_011535373.2:p.Gly632Ser
XM_011537072.2:c.1786G>A	XP_011535374.1:p.Gly596Ser
XM_017021582.1:c.2044G>A	XP_016877071.1:p.Gly682Ser
XM_017021583.1:c.2035G>A	XP_016877072.1:p.Gly679Ser
XM_017021584.1:c.1954G>A	XP_016877073.1:p.Gly652Ser
XM_017021585.1:c.1903G>A	XP_016877074.1:p.Gly635Ser
XM_017021586.1:c.1579G>A	XP_016877075.1:p.Gly527Ser
XM_017021587.1:c.1579G>A	XP_016877076.1:p.Gly527Ser
XM_017021588.1:c.1579G>A	XP_016877077.1:p.Gly527Ser
NM_001164749.2:c.1885G>A MANE Select	NP_001158221.1:p.Gly629Ser
NM_001165893.2:c.1795G>A	NP_001159365.1:p.Gly599Ser
NM_022123.3:c.1789G>A	NP_071406.1:p.Gly597Ser
NM_173159.3:c.1846G>A	NP_775182.1:p.Gly616Ser
NM_001394988.1:c.1840G>A	NP_001381917.1:p.Gly614Ser
NM_001394989.1:c.1786G>A	NP_001381918.1:p.Gly596Ser