Canonical Allele Identifier: CA389413299

Gene: NPAS3

Linked Data

• gnomAD v4: 14-33800273-A-G
• MyVariant Identifiers: chr14:g.34269479A>G (hg19) ; chr14:g.33800273A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800273A>G , CM000676.2:g.33800273A>G	GRCh38
NC_000014.8:g.34269479A>G , CM000676.1:g.34269479A>G	GRCh37
NC_000014.7:g.33339230A>G	NCBI36
NG_013036.1:g.866021A>G
NG_013036.2:g.866021A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1966A>G MANE Select	ENSP00000348460.4:p.Ile656Val
ENST00000551634.6:c.1975A>G	ENSP00000448373.2:p.Ile659Val
ENST00000680362.1:c.1866A>G
ENST00000681323.1:c.793+2692A>G
ENST00000346562.6:c.1870A>G	ENSP00000319610.5:p.Ile624Val
ENST00000356141.8:c.1966A>G	ENSP00000348460.4:p.Ile656Val
ENST00000357798.9:c.1927A>G	ENSP00000350446.5:p.Ile643Val
ENST00000548645.5:c.1876A>G	ENSP00000448916.1:p.Ile626Val
ENST00000551492.5:c.1981A>G	ENSP00000450392.1:p.Ile661Val
ENST00000551634.5:c.1888A>G	ENSP00000448373.1:p.Ile630Val
NM_001164749.1:c.1966A>G	NP_001158221.1:p.Ile656Val
NM_001165893.1:c.1876A>G	NP_001159365.1:p.Ile626Val
NM_022123.2:c.1870A>G	NP_071406.1:p.Ile624Val
NM_173159.2:c.1927A>G	NP_775182.1:p.Ile643Val
XM_005267991.2:c.1987A>G	XP_005268048.1:p.Ile663Val
XM_005267992.2:c.1981A>G	XP_005268049.1:p.Ile661Val
XM_005267993.2:c.1927A>G	XP_005268050.1:p.Ile643Val
XM_011537067.1:c.2017A>G	XP_011535369.1:p.Ile673Val
XM_011537068.1:c.2008A>G	XP_011535370.1:p.Ile670Val
XM_011537069.1:c.1978A>G	XP_011535371.1:p.Ile660Val
XM_011537070.1:c.1921A>G	XP_011535372.1:p.Ile641Val
XM_011537071.1:c.1888A>G	XP_011535373.1:p.Ile630Val
XM_011537072.1:c.1867A>G	XP_011535374.1:p.Ile623Val
XM_011537073.1:c.1660A>G	XP_011535375.1:p.Ile554Val
XM_011537074.1:c.1660A>G	XP_011535376.1:p.Ile554Val
XM_005267991.3:c.2074A>G	XP_005268048.2:p.Ile692Val
XM_005267992.3:c.2068A>G	XP_005268049.2:p.Ile690Val
XM_011537067.2:c.2017A>G	XP_011535369.1:p.Ile673Val
XM_011537069.2:c.2065A>G	XP_011535371.2:p.Ile689Val
XM_011537070.2:c.1921A>G	XP_011535372.1:p.Ile641Val
XM_011537071.2:c.1975A>G	XP_011535373.2:p.Ile659Val
XM_011537072.2:c.1867A>G	XP_011535374.1:p.Ile623Val
XM_017021582.1:c.2125A>G	XP_016877071.1:p.Ile709Val
XM_017021583.1:c.2116A>G	XP_016877072.1:p.Ile706Val
XM_017021584.1:c.2035A>G	XP_016877073.1:p.Ile679Val
XM_017021585.1:c.1984A>G	XP_016877074.1:p.Ile662Val
XM_017021586.1:c.1660A>G	XP_016877075.1:p.Ile554Val
XM_017021587.1:c.1660A>G	XP_016877076.1:p.Ile554Val
XM_017021588.1:c.1660A>G	XP_016877077.1:p.Ile554Val
NM_001164749.2:c.1966A>G MANE Select	NP_001158221.1:p.Ile656Val
NM_001165893.2:c.1876A>G	NP_001159365.1:p.Ile626Val
NM_022123.3:c.1870A>G	NP_071406.1:p.Ile624Val
NM_173159.3:c.1927A>G	NP_775182.1:p.Ile643Val
NM_001394988.1:c.1921A>G	NP_001381917.1:p.Ile641Val
NM_001394989.1:c.1867A>G	NP_001381918.1:p.Ile623Val