Canonical Allele Identifier: CA389413934

Gene: NPAS3

Linked Data

• dbSNP Id: rs1466620481
• gnomAD v2: 14-34269618-G-A
• gnomAD v4: 14-33800412-G-A
• MyVariant Identifiers: chr14:g.34269618G>A (hg19) ; chr14:g.33800412G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800412G>A , CM000676.2:g.33800412G>A	GRCh38
NC_000014.8:g.34269618G>A , CM000676.1:g.34269618G>A	GRCh37
NC_000014.7:g.33339369G>A	NCBI36
NG_013036.1:g.866160G>A
NG_013036.2:g.866160G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2105G>A MANE Select	ENSP00000348460.4:p.Gly702Asp
ENST00000551634.6:c.2114G>A	ENSP00000448373.2:p.Gly705Asp
ENST00000680362.1:c.2005G>A
ENST00000681323.1:c.793+2831G>A
ENST00000346562.6:c.2009G>A	ENSP00000319610.5:p.Gly670Asp
ENST00000356141.8:c.2105G>A	ENSP00000348460.4:p.Gly702Asp
ENST00000357798.9:c.2066G>A	ENSP00000350446.5:p.Gly689Asp
ENST00000548645.5:c.2015G>A	ENSP00000448916.1:p.Gly672Asp
ENST00000551492.5:c.2120G>A	ENSP00000450392.1:p.Gly707Asp
ENST00000551634.5:c.2027G>A	ENSP00000448373.1:p.Gly676Asp
NM_001164749.1:c.2105G>A	NP_001158221.1:p.Gly702Asp
NM_001165893.1:c.2015G>A	NP_001159365.1:p.Gly672Asp
NM_022123.2:c.2009G>A	NP_071406.1:p.Gly670Asp
NM_173159.2:c.2066G>A	NP_775182.1:p.Gly689Asp
XM_005267991.2:c.2126G>A	XP_005268048.1:p.Gly709Asp
XM_005267992.2:c.2120G>A	XP_005268049.1:p.Gly707Asp
XM_005267993.2:c.2066G>A	XP_005268050.1:p.Gly689Asp
XM_011537067.1:c.2156G>A	XP_011535369.1:p.Gly719Asp
XM_011537068.1:c.2147G>A	XP_011535370.1:p.Gly716Asp
XM_011537069.1:c.2117G>A	XP_011535371.1:p.Gly706Asp
XM_011537070.1:c.2060G>A	XP_011535372.1:p.Gly687Asp
XM_011537071.1:c.2027G>A	XP_011535373.1:p.Gly676Asp
XM_011537072.1:c.2006G>A	XP_011535374.1:p.Gly669Asp
XM_011537073.1:c.1799G>A	XP_011535375.1:p.Gly600Asp
XM_011537074.1:c.1799G>A	XP_011535376.1:p.Gly600Asp
XM_005267991.3:c.2213G>A	XP_005268048.2:p.Gly738Asp
XM_005267992.3:c.2207G>A	XP_005268049.2:p.Gly736Asp
XM_011537067.2:c.2156G>A	XP_011535369.1:p.Gly719Asp
XM_011537069.2:c.2204G>A	XP_011535371.2:p.Gly735Asp
XM_011537070.2:c.2060G>A	XP_011535372.1:p.Gly687Asp
XM_011537071.2:c.2114G>A	XP_011535373.2:p.Gly705Asp
XM_011537072.2:c.2006G>A	XP_011535374.1:p.Gly669Asp
XM_017021582.1:c.2264G>A	XP_016877071.1:p.Gly755Asp
XM_017021583.1:c.2255G>A	XP_016877072.1:p.Gly752Asp
XM_017021584.1:c.2174G>A	XP_016877073.1:p.Gly725Asp
XM_017021585.1:c.2123G>A	XP_016877074.1:p.Gly708Asp
XM_017021586.1:c.1799G>A	XP_016877075.1:p.Gly600Asp
XM_017021587.1:c.1799G>A	XP_016877076.1:p.Gly600Asp
XM_017021588.1:c.1799G>A	XP_016877077.1:p.Gly600Asp
NM_001164749.2:c.2105G>A MANE Select	NP_001158221.1:p.Gly702Asp
NM_001165893.2:c.2015G>A	NP_001159365.1:p.Gly672Asp
NM_022123.3:c.2009G>A	NP_071406.1:p.Gly670Asp
NM_173159.3:c.2066G>A	NP_775182.1:p.Gly689Asp
NM_001394988.1:c.2060G>A	NP_001381917.1:p.Gly687Asp
NM_001394989.1:c.2006G>A	NP_001381918.1:p.Gly669Asp