Canonical Allele Identifier: CA389414356

Gene: NPAS3

Linked Data

• gnomAD v4: 14-33800589-G-T
• MyVariant Identifiers: chr14:g.34269795G>T (hg19) ; chr14:g.33800589G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800589G>T , CM000676.2:g.33800589G>T	GRCh38
NC_000014.8:g.34269795G>T , CM000676.1:g.34269795G>T	GRCh37
NC_000014.7:g.33339546G>T	NCBI36
NG_013036.1:g.866337G>T
NG_013036.2:g.866337G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2282G>T MANE Select	ENSP00000348460.4:p.Gly761Val
ENST00000551634.6:c.2291G>T	ENSP00000448373.2:p.Gly764Val
ENST00000680362.1:c.2182G>T
ENST00000681323.1:c.793+3008G>T
ENST00000346562.6:c.2186G>T	ENSP00000319610.5:p.Gly729Val
ENST00000356141.8:c.2282G>T	ENSP00000348460.4:p.Gly761Val
ENST00000357798.9:c.2243G>T	ENSP00000350446.5:p.Gly748Val
ENST00000548645.5:c.2192G>T	ENSP00000448916.1:p.Gly731Val
ENST00000551492.5:c.2297G>T	ENSP00000450392.1:p.Gly766Val
ENST00000551634.5:c.2204G>T	ENSP00000448373.1:p.Gly735Val
NM_001164749.1:c.2282G>T	NP_001158221.1:p.Gly761Val
NM_001165893.1:c.2192G>T	NP_001159365.1:p.Gly731Val
NM_022123.2:c.2186G>T	NP_071406.1:p.Gly729Val
NM_173159.2:c.2243G>T	NP_775182.1:p.Gly748Val
XM_005267991.2:c.2303G>T	XP_005268048.1:p.Gly768Val
XM_005267992.2:c.2297G>T	XP_005268049.1:p.Gly766Val
XM_005267993.2:c.2243G>T	XP_005268050.1:p.Gly748Val
XM_011537067.1:c.2333G>T	XP_011535369.1:p.Gly778Val
XM_011537068.1:c.2324G>T	XP_011535370.1:p.Gly775Val
XM_011537069.1:c.2294G>T	XP_011535371.1:p.Gly765Val
XM_011537070.1:c.2237G>T	XP_011535372.1:p.Gly746Val
XM_011537071.1:c.2204G>T	XP_011535373.1:p.Gly735Val
XM_011537072.1:c.2183G>T	XP_011535374.1:p.Gly728Val
XM_011537073.1:c.1976G>T	XP_011535375.1:p.Gly659Val
XM_011537074.1:c.1976G>T	XP_011535376.1:p.Gly659Val
XM_005267991.3:c.2390G>T	XP_005268048.2:p.Gly797Val
XM_005267992.3:c.2384G>T	XP_005268049.2:p.Gly795Val
XM_011537067.2:c.2333G>T	XP_011535369.1:p.Gly778Val
XM_011537069.2:c.2381G>T	XP_011535371.2:p.Gly794Val
XM_011537070.2:c.2237G>T	XP_011535372.1:p.Gly746Val
XM_011537071.2:c.2291G>T	XP_011535373.2:p.Gly764Val
XM_011537072.2:c.2183G>T	XP_011535374.1:p.Gly728Val
XM_017021582.1:c.2441G>T	XP_016877071.1:p.Gly814Val
XM_017021583.1:c.2432G>T	XP_016877072.1:p.Gly811Val
XM_017021584.1:c.2351G>T	XP_016877073.1:p.Gly784Val
XM_017021585.1:c.2300G>T	XP_016877074.1:p.Gly767Val
XM_017021586.1:c.1976G>T	XP_016877075.1:p.Gly659Val
XM_017021587.1:c.1976G>T	XP_016877076.1:p.Gly659Val
XM_017021588.1:c.1976G>T	XP_016877077.1:p.Gly659Val
NM_001164749.2:c.2282G>T MANE Select	NP_001158221.1:p.Gly761Val
NM_001165893.2:c.2192G>T	NP_001159365.1:p.Gly731Val
NM_022123.3:c.2186G>T	NP_071406.1:p.Gly729Val
NM_173159.3:c.2243G>T	NP_775182.1:p.Gly748Val
NM_001394988.1:c.2237G>T	NP_001381917.1:p.Gly746Val
NM_001394989.1:c.2183G>T	NP_001381918.1:p.Gly728Val