Canonical Allele Identifier: CA486093097

Gene: NPAS3

Linked Data

• gnomAD v4: 14-33800398-C-A
• MyVariant Identifiers: chr14:g.34269604C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800398C>A , CM000676.2:g.33800398C>A	GRCh38
NC_000014.8:g.34269604C>A , CM000676.1:g.34269604C>A	GRCh37
NC_000014.7:g.33339355C>A	NCBI36
NG_013036.1:g.866146C>A
NG_013036.2:g.866146C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2091C>A MANE Select	ENSP00000348460.4:p.Gly697=
ENST00000551634.6:c.2100C>A	ENSP00000448373.2:p.Gly700=
ENST00000680362.1:c.1991C>A
ENST00000681323.1:c.793+2817C>A
ENST00000346562.6:c.1995C>A	ENSP00000319610.5:p.Gly665=
ENST00000356141.8:c.2091C>A	ENSP00000348460.4:p.Gly697=
ENST00000357798.9:c.2052C>A	ENSP00000350446.5:p.Gly684=
ENST00000548645.5:c.2001C>A	ENSP00000448916.1:p.Gly667=
ENST00000551492.5:c.2106C>A	ENSP00000450392.1:p.Gly702=
ENST00000551634.5:c.2013C>A	ENSP00000448373.1:p.Gly671=
NM_001164749.1:c.2091C>A	NP_001158221.1:p.Gly697=
NM_001165893.1:c.2001C>A	NP_001159365.1:p.Gly667=
NM_022123.2:c.1995C>A	NP_071406.1:p.Gly665=
NM_173159.2:c.2052C>A	NP_775182.1:p.Gly684=
XM_005267991.2:c.2112C>A	XP_005268048.1:p.Gly704=
XM_005267992.2:c.2106C>A	XP_005268049.1:p.Gly702=
XM_005267993.2:c.2052C>A	XP_005268050.1:p.Gly684=
XM_011537067.1:c.2142C>A	XP_011535369.1:p.Gly714=
XM_011537068.1:c.2133C>A	XP_011535370.1:p.Gly711=
XM_011537069.1:c.2103C>A	XP_011535371.1:p.Gly701=
XM_011537070.1:c.2046C>A	XP_011535372.1:p.Gly682=
XM_011537071.1:c.2013C>A	XP_011535373.1:p.Gly671=
XM_011537072.1:c.1992C>A	XP_011535374.1:p.Gly664=
XM_011537073.1:c.1785C>A	XP_011535375.1:p.Gly595=
XM_011537074.1:c.1785C>A	XP_011535376.1:p.Gly595=
XM_005267991.3:c.2199C>A	XP_005268048.2:p.Gly733=
XM_005267992.3:c.2193C>A	XP_005268049.2:p.Gly731=
XM_011537067.2:c.2142C>A	XP_011535369.1:p.Gly714=
XM_011537069.2:c.2190C>A	XP_011535371.2:p.Gly730=
XM_011537070.2:c.2046C>A	XP_011535372.1:p.Gly682=
XM_011537071.2:c.2100C>A	XP_011535373.2:p.Gly700=
XM_011537072.2:c.1992C>A	XP_011535374.1:p.Gly664=
XM_017021582.1:c.2250C>A	XP_016877071.1:p.Gly750=
XM_017021583.1:c.2241C>A	XP_016877072.1:p.Gly747=
XM_017021584.1:c.2160C>A	XP_016877073.1:p.Gly720=
XM_017021585.1:c.2109C>A	XP_016877074.1:p.Gly703=
XM_017021586.1:c.1785C>A	XP_016877075.1:p.Gly595=
XM_017021587.1:c.1785C>A	XP_016877076.1:p.Gly595=
XM_017021588.1:c.1785C>A	XP_016877077.1:p.Gly595=
NM_001164749.2:c.2091C>A MANE Select	NP_001158221.1:p.Gly697=
NM_001165893.2:c.2001C>A	NP_001159365.1:p.Gly667=
NM_022123.3:c.1995C>A	NP_071406.1:p.Gly665=
NM_173159.3:c.2052C>A	NP_775182.1:p.Gly684=
NM_001394988.1:c.2046C>A	NP_001381917.1:p.Gly682=
NM_001394989.1:c.1992C>A	NP_001381918.1:p.Gly664=