Canonical Allele Identifier: CA14028512

Gene: NPAS3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33241581T>C , CM000676.2:g.33241581T>C	GRCh38
NC_000014.8:g.33710787T>C , CM000676.1:g.33710787T>C	GRCh37
NC_000014.7:g.32780538T>C	NCBI36
NG_013036.1:g.307329T>C
NG_013036.2:g.307329T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.385+26155T>C MANE Select	ENSP00000348460.4:n.385+26155T>C
ENST00000551008.6:c.214+26155T>C	ENSP00000447213.2:n.214+26155T>C
ENST00000551634.6:c.403+26155T>C	ENSP00000448373.2:n.403+26155T>C
ENST00000680362.1:c.245+26155T>C
ENST00000681796.1:n.236+26155T>C
ENST00000346562.6:c.295+26155T>C	ENSP00000319610.5:n.295+26155T>C
ENST00000356141.8:c.385+26155T>C	ENSP00000348460.4:n.385+26155T>C
ENST00000357798.9:c.346+25994T>C	ENSP00000350446.5:n.346+25994T>C
ENST00000546849.1:c.115+26155T>C	ENSP00000446700.1:n.115+26155T>C
ENST00000547068.5:c.79+26155T>C	ENSP00000449542.1:n.79+26155T>C
ENST00000548645.5:c.295+26155T>C	ENSP00000448916.1:n.295+26155T>C
ENST00000549770.1:n.245+26155T>C
ENST00000551008.5:c.79+26155T>C	ENSP00000447213.1:n.79+26155T>C
ENST00000551492.5:c.406+26155T>C	ENSP00000450392.1:n.406+26155T>C
ENST00000551634.5:c.316+26155T>C	ENSP00000448373.1:n.316+26155T>C
NM_001164749.1:c.385+26155T>C	NP_001158221.1:n.385+26155T>C
NM_001165893.1:c.295+26155T>C	NP_001159365.1:n.295+26155T>C
NM_022123.2:c.295+26155T>C	NP_071406.1:n.295+26155T>C
NM_173159.2:c.346+25994T>C	NP_775182.1:n.346+25994T>C
XM_005267991.2:c.406+26155T>C	XP_005268048.1:n.406+26155T>C
XM_005267992.2:c.406+26155T>C	XP_005268049.1:n.406+26155T>C
XM_005267993.2:c.346+25994T>C	XP_005268050.1:n.346+25994T>C
XM_011537067.1:c.436+25994T>C	XP_011535369.1:n.436+25994T>C
XM_011537068.1:c.436+25994T>C	XP_011535370.1:n.436+25994T>C
XM_011537069.1:c.406+26155T>C	XP_011535371.1:n.406+26155T>C
XM_011537070.1:c.346+25994T>C	XP_011535372.1:n.346+25994T>C
XM_011537071.1:c.316+26155T>C	XP_011535373.1:n.316+26155T>C
XM_011537072.1:c.295+26155T>C	XP_011535374.1:n.295+26155T>C
XM_011537073.1:c.79+26155T>C	XP_011535375.1:n.79+26155T>C
XM_011537074.1:c.79+26155T>C	XP_011535376.1:n.79+26155T>C
XM_005267991.3:c.493+26155T>C	XP_005268048.2:n.493+26155T>C
XM_005267992.3:c.493+26155T>C	XP_005268049.2:n.493+26155T>C
XM_011537067.2:c.436+25994T>C	XP_011535369.1:n.436+25994T>C
XM_011537069.2:c.493+26155T>C	XP_011535371.2:n.493+26155T>C
XM_011537070.2:c.346+25994T>C	XP_011535372.1:n.346+25994T>C
XM_011537071.2:c.403+26155T>C	XP_011535373.2:n.403+26155T>C
XM_011537072.2:c.295+26155T>C	XP_011535374.1:n.295+26155T>C
XM_017021582.1:c.544+25994T>C	XP_016877071.1:n.544+25994T>C
XM_017021583.1:c.544+25994T>C	XP_016877072.1:n.544+25994T>C
XM_017021584.1:c.454+25994T>C	XP_016877073.1:n.454+25994T>C
XM_017021585.1:c.403+26155T>C	XP_016877074.1:n.403+26155T>C
XM_017021586.1:c.79+26155T>C	XP_016877075.1:n.79+26155T>C
XM_017021587.1:c.79+26155T>C	XP_016877076.1:n.79+26155T>C
XM_017021588.1:c.79+26155T>C	XP_016877077.1:n.79+26155T>C
NM_001164749.2:c.385+26155T>C MANE Select	NP_001158221.1:n.385+26155T>C
NM_001165893.2:c.295+26155T>C	NP_001159365.1:n.295+26155T>C
NM_022123.3:c.295+26155T>C	NP_071406.1:n.295+26155T>C
NM_173159.3:c.346+25994T>C	NP_775182.1:n.346+25994T>C
NM_001394988.1:c.346+25994T>C	NP_001381917.1:n.346+25994T>C
NM_001394989.1:c.295+26155T>C	NP_001381918.1:n.295+26155T>C