Canonical Allele Identifier: CA389414326

Gene: NPAS3

Linked Data

• gnomAD v4: 14-33800577-A-G
• MyVariant Identifiers: chr14:g.34269783A>G (hg19) ; chr14:g.33800577A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800577A>G , CM000676.2:g.33800577A>G	GRCh38
NC_000014.8:g.34269783A>G , CM000676.1:g.34269783A>G	GRCh37
NC_000014.7:g.33339534A>G	NCBI36
NG_013036.1:g.866325A>G
NG_013036.2:g.866325A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2270A>G MANE Select	ENSP00000348460.4:p.Asp757Gly
ENST00000551634.6:c.2279A>G	ENSP00000448373.2:p.Asp760Gly
ENST00000680362.1:c.2170A>G
ENST00000681323.1:c.793+2996A>G
ENST00000346562.6:c.2174A>G	ENSP00000319610.5:p.Asp725Gly
ENST00000356141.8:c.2270A>G	ENSP00000348460.4:p.Asp757Gly
ENST00000357798.9:c.2231A>G	ENSP00000350446.5:p.Asp744Gly
ENST00000548645.5:c.2180A>G	ENSP00000448916.1:p.Asp727Gly
ENST00000551492.5:c.2285A>G	ENSP00000450392.1:p.Asp762Gly
ENST00000551634.5:c.2192A>G	ENSP00000448373.1:p.Asp731Gly
NM_001164749.1:c.2270A>G	NP_001158221.1:p.Asp757Gly
NM_001165893.1:c.2180A>G	NP_001159365.1:p.Asp727Gly
NM_022123.2:c.2174A>G	NP_071406.1:p.Asp725Gly
NM_173159.2:c.2231A>G	NP_775182.1:p.Asp744Gly
XM_005267991.2:c.2291A>G	XP_005268048.1:p.Asp764Gly
XM_005267992.2:c.2285A>G	XP_005268049.1:p.Asp762Gly
XM_005267993.2:c.2231A>G	XP_005268050.1:p.Asp744Gly
XM_011537067.1:c.2321A>G	XP_011535369.1:p.Asp774Gly
XM_011537068.1:c.2312A>G	XP_011535370.1:p.Asp771Gly
XM_011537069.1:c.2282A>G	XP_011535371.1:p.Asp761Gly
XM_011537070.1:c.2225A>G	XP_011535372.1:p.Asp742Gly
XM_011537071.1:c.2192A>G	XP_011535373.1:p.Asp731Gly
XM_011537072.1:c.2171A>G	XP_011535374.1:p.Asp724Gly
XM_011537073.1:c.1964A>G	XP_011535375.1:p.Asp655Gly
XM_011537074.1:c.1964A>G	XP_011535376.1:p.Asp655Gly
XM_005267991.3:c.2378A>G	XP_005268048.2:p.Asp793Gly
XM_005267992.3:c.2372A>G	XP_005268049.2:p.Asp791Gly
XM_011537067.2:c.2321A>G	XP_011535369.1:p.Asp774Gly
XM_011537069.2:c.2369A>G	XP_011535371.2:p.Asp790Gly
XM_011537070.2:c.2225A>G	XP_011535372.1:p.Asp742Gly
XM_011537071.2:c.2279A>G	XP_011535373.2:p.Asp760Gly
XM_011537072.2:c.2171A>G	XP_011535374.1:p.Asp724Gly
XM_017021582.1:c.2429A>G	XP_016877071.1:p.Asp810Gly
XM_017021583.1:c.2420A>G	XP_016877072.1:p.Asp807Gly
XM_017021584.1:c.2339A>G	XP_016877073.1:p.Asp780Gly
XM_017021585.1:c.2288A>G	XP_016877074.1:p.Asp763Gly
XM_017021586.1:c.1964A>G	XP_016877075.1:p.Asp655Gly
XM_017021587.1:c.1964A>G	XP_016877076.1:p.Asp655Gly
XM_017021588.1:c.1964A>G	XP_016877077.1:p.Asp655Gly
NM_001164749.2:c.2270A>G MANE Select	NP_001158221.1:p.Asp757Gly
NM_001165893.2:c.2180A>G	NP_001159365.1:p.Asp727Gly
NM_022123.3:c.2174A>G	NP_071406.1:p.Asp725Gly
NM_173159.3:c.2231A>G	NP_775182.1:p.Asp744Gly
NM_001394988.1:c.2225A>G	NP_001381917.1:p.Asp742Gly
NM_001394989.1:c.2171A>G	NP_001381918.1:p.Asp724Gly