Canonical Allele Identifier: CA389414140

Gene: NPAS3

Linked Data

• dbSNP Id: rs1380884687
• gnomAD v3: 14-33800484-C-A
• gnomAD v4: 14-33800484-C-A
• MyVariant Identifiers: chr14:g.34269690C>A (hg19) ; chr14:g.33800484C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800484C>A , CM000676.2:g.33800484C>A	GRCh38
NC_000014.8:g.34269690C>A , CM000676.1:g.34269690C>A	GRCh37
NC_000014.7:g.33339441C>A	NCBI36
NG_013036.1:g.866232C>A
NG_013036.2:g.866232C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000356141.9:c.2177C>A MANE Select	ENSP00000348460.4:p.Ala726Asp
ENST00000551634.6:c.2186C>A	ENSP00000448373.2:p.Ala729Asp
ENST00000680362.1:c.2077C>A
ENST00000681323.1:c.793+2903C>A
ENST00000346562.6:c.2081C>A	ENSP00000319610.5:p.Ala694Asp
ENST00000356141.8:c.2177C>A	ENSP00000348460.4:p.Ala726Asp
ENST00000357798.9:c.2138C>A	ENSP00000350446.5:p.Ala713Asp
ENST00000548645.5:c.2087C>A	ENSP00000448916.1:p.Ala696Asp
ENST00000551492.5:c.2192C>A	ENSP00000450392.1:p.Ala731Asp
ENST00000551634.5:c.2099C>A	ENSP00000448373.1:p.Ala700Asp
NM_001164749.1:c.2177C>A	NP_001158221.1:p.Ala726Asp
NM_001165893.1:c.2087C>A	NP_001159365.1:p.Ala696Asp
NM_022123.2:c.2081C>A	NP_071406.1:p.Ala694Asp
NM_173159.2:c.2138C>A	NP_775182.1:p.Ala713Asp
XM_005267991.2:c.2198C>A	XP_005268048.1:p.Ala733Asp
XM_005267992.2:c.2192C>A	XP_005268049.1:p.Ala731Asp
XM_005267993.2:c.2138C>A	XP_005268050.1:p.Ala713Asp
XM_011537067.1:c.2228C>A	XP_011535369.1:p.Ala743Asp
XM_011537068.1:c.2219C>A	XP_011535370.1:p.Ala740Asp
XM_011537069.1:c.2189C>A	XP_011535371.1:p.Ala730Asp
XM_011537070.1:c.2132C>A	XP_011535372.1:p.Ala711Asp
XM_011537071.1:c.2099C>A	XP_011535373.1:p.Ala700Asp
XM_011537072.1:c.2078C>A	XP_011535374.1:p.Ala693Asp
XM_011537073.1:c.1871C>A	XP_011535375.1:p.Ala624Asp
XM_011537074.1:c.1871C>A	XP_011535376.1:p.Ala624Asp
XM_005267991.3:c.2285C>A	XP_005268048.2:p.Ala762Asp
XM_005267992.3:c.2279C>A	XP_005268049.2:p.Ala760Asp
XM_011537067.2:c.2228C>A	XP_011535369.1:p.Ala743Asp
XM_011537069.2:c.2276C>A	XP_011535371.2:p.Ala759Asp
XM_011537070.2:c.2132C>A	XP_011535372.1:p.Ala711Asp
XM_011537071.2:c.2186C>A	XP_011535373.2:p.Ala729Asp
XM_011537072.2:c.2078C>A	XP_011535374.1:p.Ala693Asp
XM_017021582.1:c.2336C>A	XP_016877071.1:p.Ala779Asp
XM_017021583.1:c.2327C>A	XP_016877072.1:p.Ala776Asp
XM_017021584.1:c.2246C>A	XP_016877073.1:p.Ala749Asp
XM_017021585.1:c.2195C>A	XP_016877074.1:p.Ala732Asp
XM_017021586.1:c.1871C>A	XP_016877075.1:p.Ala624Asp
XM_017021587.1:c.1871C>A	XP_016877076.1:p.Ala624Asp
XM_017021588.1:c.1871C>A	XP_016877077.1:p.Ala624Asp
NM_001164749.2:c.2177C>A MANE Select	NP_001158221.1:p.Ala726Asp
NM_001165893.2:c.2087C>A	NP_001159365.1:p.Ala696Asp
NM_022123.3:c.2081C>A	NP_071406.1:p.Ala694Asp
NM_173159.3:c.2138C>A	NP_775182.1:p.Ala713Asp
NM_001394988.1:c.2132C>A	NP_001381917.1:p.Ala711Asp
NM_001394989.1:c.2078C>A	NP_001381918.1:p.Ala693Asp