Canonical Allele Identifier: CA389414116

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269678A>C (hg19) ; chr14:g.33800472A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800472A>C , CM000676.2:g.33800472A>C	GRCh38
NC_000014.8:g.34269678A>C , CM000676.1:g.34269678A>C	GRCh37
NC_000014.7:g.33339429A>C	NCBI36
NG_013036.1:g.866220A>C
NG_013036.2:g.866220A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000356141.9:c.2165A>C MANE Select	ENSP00000348460.4:p.Asp722Ala
ENST00000551634.6:c.2174A>C	ENSP00000448373.2:p.Asp725Ala
ENST00000680362.1:c.2065A>C
ENST00000681323.1:c.793+2891A>C
ENST00000346562.6:c.2069A>C	ENSP00000319610.5:p.Asp690Ala
ENST00000356141.8:c.2165A>C	ENSP00000348460.4:p.Asp722Ala
ENST00000357798.9:c.2126A>C	ENSP00000350446.5:p.Asp709Ala
ENST00000548645.5:c.2075A>C	ENSP00000448916.1:p.Asp692Ala
ENST00000551492.5:c.2180A>C	ENSP00000450392.1:p.Asp727Ala
ENST00000551634.5:c.2087A>C	ENSP00000448373.1:p.Asp696Ala
NM_001164749.1:c.2165A>C	NP_001158221.1:p.Asp722Ala
NM_001165893.1:c.2075A>C	NP_001159365.1:p.Asp692Ala
NM_022123.2:c.2069A>C	NP_071406.1:p.Asp690Ala
NM_173159.2:c.2126A>C	NP_775182.1:p.Asp709Ala
XM_005267991.2:c.2186A>C	XP_005268048.1:p.Asp729Ala
XM_005267992.2:c.2180A>C	XP_005268049.1:p.Asp727Ala
XM_005267993.2:c.2126A>C	XP_005268050.1:p.Asp709Ala
XM_011537067.1:c.2216A>C	XP_011535369.1:p.Asp739Ala
XM_011537068.1:c.2207A>C	XP_011535370.1:p.Asp736Ala
XM_011537069.1:c.2177A>C	XP_011535371.1:p.Asp726Ala
XM_011537070.1:c.2120A>C	XP_011535372.1:p.Asp707Ala
XM_011537071.1:c.2087A>C	XP_011535373.1:p.Asp696Ala
XM_011537072.1:c.2066A>C	XP_011535374.1:p.Asp689Ala
XM_011537073.1:c.1859A>C	XP_011535375.1:p.Asp620Ala
XM_011537074.1:c.1859A>C	XP_011535376.1:p.Asp620Ala
XM_005267991.3:c.2273A>C	XP_005268048.2:p.Asp758Ala
XM_005267992.3:c.2267A>C	XP_005268049.2:p.Asp756Ala
XM_011537067.2:c.2216A>C	XP_011535369.1:p.Asp739Ala
XM_011537069.2:c.2264A>C	XP_011535371.2:p.Asp755Ala
XM_011537070.2:c.2120A>C	XP_011535372.1:p.Asp707Ala
XM_011537071.2:c.2174A>C	XP_011535373.2:p.Asp725Ala
XM_011537072.2:c.2066A>C	XP_011535374.1:p.Asp689Ala
XM_017021582.1:c.2324A>C	XP_016877071.1:p.Asp775Ala
XM_017021583.1:c.2315A>C	XP_016877072.1:p.Asp772Ala
XM_017021584.1:c.2234A>C	XP_016877073.1:p.Asp745Ala
XM_017021585.1:c.2183A>C	XP_016877074.1:p.Asp728Ala
XM_017021586.1:c.1859A>C	XP_016877075.1:p.Asp620Ala
XM_017021587.1:c.1859A>C	XP_016877076.1:p.Asp620Ala
XM_017021588.1:c.1859A>C	XP_016877077.1:p.Asp620Ala
NM_001164749.2:c.2165A>C MANE Select	NP_001158221.1:p.Asp722Ala
NM_001165893.2:c.2075A>C	NP_001159365.1:p.Asp692Ala
NM_022123.3:c.2069A>C	NP_071406.1:p.Asp690Ala
NM_173159.3:c.2126A>C	NP_775182.1:p.Asp709Ala
NM_001394988.1:c.2120A>C	NP_001381917.1:p.Asp707Ala
NM_001394989.1:c.2066A>C	NP_001381918.1:p.Asp689Ala