Canonical Allele Identifier: CA389414066

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269652C>G (hg19) ; chr14:g.33800446C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800446C>G , CM000676.2:g.33800446C>G	GRCh38
NC_000014.8:g.34269652C>G , CM000676.1:g.34269652C>G	GRCh37
NC_000014.7:g.33339403C>G	NCBI36
NG_013036.1:g.866194C>G
NG_013036.2:g.866194C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2139C>G MANE Select	ENSP00000348460.4:p.Asp713Glu
ENST00000551634.6:c.2148C>G	ENSP00000448373.2:p.Asp716Glu
ENST00000680362.1:c.2039C>G
ENST00000681323.1:c.793+2865C>G
ENST00000346562.6:c.2043C>G	ENSP00000319610.5:p.Asp681Glu
ENST00000356141.8:c.2139C>G	ENSP00000348460.4:p.Asp713Glu
ENST00000357798.9:c.2100C>G	ENSP00000350446.5:p.Asp700Glu
ENST00000548645.5:c.2049C>G	ENSP00000448916.1:p.Asp683Glu
ENST00000551492.5:c.2154C>G	ENSP00000450392.1:p.Asp718Glu
ENST00000551634.5:c.2061C>G	ENSP00000448373.1:p.Asp687Glu
NM_001164749.1:c.2139C>G	NP_001158221.1:p.Asp713Glu
NM_001165893.1:c.2049C>G	NP_001159365.1:p.Asp683Glu
NM_022123.2:c.2043C>G	NP_071406.1:p.Asp681Glu
NM_173159.2:c.2100C>G	NP_775182.1:p.Asp700Glu
XM_005267991.2:c.2160C>G	XP_005268048.1:p.Asp720Glu
XM_005267992.2:c.2154C>G	XP_005268049.1:p.Asp718Glu
XM_005267993.2:c.2100C>G	XP_005268050.1:p.Asp700Glu
XM_011537067.1:c.2190C>G	XP_011535369.1:p.Asp730Glu
XM_011537068.1:c.2181C>G	XP_011535370.1:p.Asp727Glu
XM_011537069.1:c.2151C>G	XP_011535371.1:p.Asp717Glu
XM_011537070.1:c.2094C>G	XP_011535372.1:p.Asp698Glu
XM_011537071.1:c.2061C>G	XP_011535373.1:p.Asp687Glu
XM_011537072.1:c.2040C>G	XP_011535374.1:p.Asp680Glu
XM_011537073.1:c.1833C>G	XP_011535375.1:p.Asp611Glu
XM_011537074.1:c.1833C>G	XP_011535376.1:p.Asp611Glu
XM_005267991.3:c.2247C>G	XP_005268048.2:p.Asp749Glu
XM_005267992.3:c.2241C>G	XP_005268049.2:p.Asp747Glu
XM_011537067.2:c.2190C>G	XP_011535369.1:p.Asp730Glu
XM_011537069.2:c.2238C>G	XP_011535371.2:p.Asp746Glu
XM_011537070.2:c.2094C>G	XP_011535372.1:p.Asp698Glu
XM_011537071.2:c.2148C>G	XP_011535373.2:p.Asp716Glu
XM_011537072.2:c.2040C>G	XP_011535374.1:p.Asp680Glu
XM_017021582.1:c.2298C>G	XP_016877071.1:p.Asp766Glu
XM_017021583.1:c.2289C>G	XP_016877072.1:p.Asp763Glu
XM_017021584.1:c.2208C>G	XP_016877073.1:p.Asp736Glu
XM_017021585.1:c.2157C>G	XP_016877074.1:p.Asp719Glu
XM_017021586.1:c.1833C>G	XP_016877075.1:p.Asp611Glu
XM_017021587.1:c.1833C>G	XP_016877076.1:p.Asp611Glu
XM_017021588.1:c.1833C>G	XP_016877077.1:p.Asp611Glu
NM_001164749.2:c.2139C>G MANE Select	NP_001158221.1:p.Asp713Glu
NM_001165893.2:c.2049C>G	NP_001159365.1:p.Asp683Glu
NM_022123.3:c.2043C>G	NP_071406.1:p.Asp681Glu
NM_173159.3:c.2100C>G	NP_775182.1:p.Asp700Glu
NM_001394988.1:c.2094C>G	NP_001381917.1:p.Asp698Glu
NM_001394989.1:c.2040C>G	NP_001381918.1:p.Asp680Glu