Canonical Allele Identifier: CA2128228740

Gene: NPAS3

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33599495A>G , CM000676.2:g.33599495A>G	GRCh38
NC_000014.8:g.34068701A>G , CM000676.1:g.34068701A>G	GRCh37
NC_000014.7:g.33138452A>G	NCBI36
NG_013036.1:g.665243A>G
NG_013036.2:g.665243A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.558+39285A>G MANE Select	ENSP00000348460.4:n.558+39285A>G
ENST00000551008.6:c.387+39285A>G	ENSP00000447213.2:n.387+39285A>G
ENST00000551634.6:c.576+39285A>G	ENSP00000448373.2:n.576+39285A>G
ENST00000680362.1:c.458+39285A>G
ENST00000346562.6:c.462+39285A>G	ENSP00000319610.5:n.462+39285A>G
ENST00000356141.8:c.558+39285A>G	ENSP00000348460.4:n.558+39285A>G
ENST00000357798.9:c.519+39285A>G	ENSP00000350446.5:n.519+39285A>G
ENST00000546849.1:c.289-12910A>G	ENSP00000446700.1:n.289-12910A>G
ENST00000547068.5:c.246+39285A>G	ENSP00000449542.1:n.246+39285A>G
ENST00000548645.5:c.468+39285A>G	ENSP00000448916.1:n.468+39285A>G
ENST00000551008.5:c.252+39285A>G	ENSP00000447213.1:n.252+39285A>G
ENST00000551492.5:c.573+39285A>G	ENSP00000450392.1:n.573+39285A>G
ENST00000551634.5:c.489+39285A>G	ENSP00000448373.1:n.489+39285A>G
NM_001164749.1:c.558+39285A>G	NP_001158221.1:n.558+39285A>G
NM_001165893.1:c.468+39285A>G	NP_001159365.1:n.468+39285A>G
NM_022123.2:c.462+39285A>G	NP_071406.1:n.462+39285A>G
NM_173159.2:c.519+39285A>G	NP_775182.1:n.519+39285A>G
XM_005267991.2:c.579+39285A>G	XP_005268048.1:n.579+39285A>G
XM_005267992.2:c.573+39285A>G	XP_005268049.1:n.573+39285A>G
XM_005267993.2:c.519+39285A>G	XP_005268050.1:n.519+39285A>G
XM_011537067.1:c.609+39285A>G	XP_011535369.1:n.609+39285A>G
XM_011537068.1:c.609+39285A>G	XP_011535370.1:n.609+39285A>G
XM_011537069.1:c.579+39285A>G	XP_011535371.1:n.579+39285A>G
XM_011537070.1:c.513+39285A>G	XP_011535372.1:n.513+39285A>G
XM_011537071.1:c.489+39285A>G	XP_011535373.1:n.489+39285A>G
XM_011537072.1:c.468+39285A>G	XP_011535374.1:n.468+39285A>G
XM_011537073.1:c.252+39285A>G	XP_011535375.1:n.252+39285A>G
XM_011537074.1:c.252+39285A>G	XP_011535376.1:n.252+39285A>G
XM_005267991.3:c.666+39285A>G	XP_005268048.2:n.666+39285A>G
XM_005267992.3:c.660+39285A>G	XP_005268049.2:n.660+39285A>G
XM_011537067.2:c.609+39285A>G	XP_011535369.1:n.609+39285A>G
XM_011537069.2:c.666+39285A>G	XP_011535371.2:n.666+39285A>G
XM_011537070.2:c.513+39285A>G	XP_011535372.1:n.513+39285A>G
XM_011537071.2:c.576+39285A>G	XP_011535373.2:n.576+39285A>G
XM_011537072.2:c.468+39285A>G	XP_011535374.1:n.468+39285A>G
XM_017021582.1:c.717+39285A>G	XP_016877071.1:n.717+39285A>G
XM_017021583.1:c.717+39285A>G	XP_016877072.1:n.717+39285A>G
XM_017021584.1:c.627+39285A>G	XP_016877073.1:n.627+39285A>G
XM_017021585.1:c.576+39285A>G	XP_016877074.1:n.576+39285A>G
XM_017021586.1:c.252+39285A>G	XP_016877075.1:n.252+39285A>G
XM_017021587.1:c.252+39285A>G	XP_016877076.1:n.252+39285A>G
XM_017021588.1:c.252+39285A>G	XP_016877077.1:n.252+39285A>G
NM_001164749.2:c.558+39285A>G MANE Select	NP_001158221.1:n.558+39285A>G
NM_001165893.2:c.468+39285A>G	NP_001159365.1:n.468+39285A>G
NM_022123.3:c.462+39285A>G	NP_071406.1:n.462+39285A>G
NM_173159.3:c.519+39285A>G	NP_775182.1:n.519+39285A>G
NM_001394988.1:c.513+39285A>G	NP_001381917.1:n.513+39285A>G
NM_001394989.1:c.468+39285A>G	NP_001381918.1:n.468+39285A>G