Canonical Allele Identifier: CA389414128

Gene: NPAS3

Linked Data

• dbSNP Id: rs1455593550
• gnomAD v2: 14-34269684-C-A
• gnomAD v4: 14-33800478-C-A
• MyVariant Identifiers: chr14:g.34269684C>A (hg19) ; chr14:g.33800478C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800478C>A , CM000676.2:g.33800478C>A	GRCh38
NC_000014.8:g.34269684C>A , CM000676.1:g.34269684C>A	GRCh37
NC_000014.7:g.33339435C>A	NCBI36
NG_013036.1:g.866226C>A
NG_013036.2:g.866226C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000356141.9:c.2171C>A MANE Select	ENSP00000348460.4:p.Ala724Glu
ENST00000551634.6:c.2180C>A	ENSP00000448373.2:p.Ala727Glu
ENST00000680362.1:c.2071C>A
ENST00000681323.1:c.793+2897C>A
ENST00000346562.6:c.2075C>A	ENSP00000319610.5:p.Ala692Glu
ENST00000356141.8:c.2171C>A	ENSP00000348460.4:p.Ala724Glu
ENST00000357798.9:c.2132C>A	ENSP00000350446.5:p.Ala711Glu
ENST00000548645.5:c.2081C>A	ENSP00000448916.1:p.Ala694Glu
ENST00000551492.5:c.2186C>A	ENSP00000450392.1:p.Ala729Glu
ENST00000551634.5:c.2093C>A	ENSP00000448373.1:p.Ala698Glu
NM_001164749.1:c.2171C>A	NP_001158221.1:p.Ala724Glu
NM_001165893.1:c.2081C>A	NP_001159365.1:p.Ala694Glu
NM_022123.2:c.2075C>A	NP_071406.1:p.Ala692Glu
NM_173159.2:c.2132C>A	NP_775182.1:p.Ala711Glu
XM_005267991.2:c.2192C>A	XP_005268048.1:p.Ala731Glu
XM_005267992.2:c.2186C>A	XP_005268049.1:p.Ala729Glu
XM_005267993.2:c.2132C>A	XP_005268050.1:p.Ala711Glu
XM_011537067.1:c.2222C>A	XP_011535369.1:p.Ala741Glu
XM_011537068.1:c.2213C>A	XP_011535370.1:p.Ala738Glu
XM_011537069.1:c.2183C>A	XP_011535371.1:p.Ala728Glu
XM_011537070.1:c.2126C>A	XP_011535372.1:p.Ala709Glu
XM_011537071.1:c.2093C>A	XP_011535373.1:p.Ala698Glu
XM_011537072.1:c.2072C>A	XP_011535374.1:p.Ala691Glu
XM_011537073.1:c.1865C>A	XP_011535375.1:p.Ala622Glu
XM_011537074.1:c.1865C>A	XP_011535376.1:p.Ala622Glu
XM_005267991.3:c.2279C>A	XP_005268048.2:p.Ala760Glu
XM_005267992.3:c.2273C>A	XP_005268049.2:p.Ala758Glu
XM_011537067.2:c.2222C>A	XP_011535369.1:p.Ala741Glu
XM_011537069.2:c.2270C>A	XP_011535371.2:p.Ala757Glu
XM_011537070.2:c.2126C>A	XP_011535372.1:p.Ala709Glu
XM_011537071.2:c.2180C>A	XP_011535373.2:p.Ala727Glu
XM_011537072.2:c.2072C>A	XP_011535374.1:p.Ala691Glu
XM_017021582.1:c.2330C>A	XP_016877071.1:p.Ala777Glu
XM_017021583.1:c.2321C>A	XP_016877072.1:p.Ala774Glu
XM_017021584.1:c.2240C>A	XP_016877073.1:p.Ala747Glu
XM_017021585.1:c.2189C>A	XP_016877074.1:p.Ala730Glu
XM_017021586.1:c.1865C>A	XP_016877075.1:p.Ala622Glu
XM_017021587.1:c.1865C>A	XP_016877076.1:p.Ala622Glu
XM_017021588.1:c.1865C>A	XP_016877077.1:p.Ala622Glu
NM_001164749.2:c.2171C>A MANE Select	NP_001158221.1:p.Ala724Glu
NM_001165893.2:c.2081C>A	NP_001159365.1:p.Ala694Glu
NM_022123.3:c.2075C>A	NP_071406.1:p.Ala692Glu
NM_173159.3:c.2132C>A	NP_775182.1:p.Ala711Glu
NM_001394988.1:c.2126C>A	NP_001381917.1:p.Ala709Glu
NM_001394989.1:c.2072C>A	NP_001381918.1:p.Ala691Glu