Canonical Allele Identifier: CA389413918

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269615G>C (hg19) ; chr14:g.33800409G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800409G>C , CM000676.2:g.33800409G>C	GRCh38
NC_000014.8:g.34269615G>C , CM000676.1:g.34269615G>C	GRCh37
NC_000014.7:g.33339366G>C	NCBI36
NG_013036.1:g.866157G>C
NG_013036.2:g.866157G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2102G>C MANE Select	ENSP00000348460.4:p.Gly701Ala
ENST00000551634.6:c.2111G>C	ENSP00000448373.2:p.Gly704Ala
ENST00000680362.1:c.2002G>C
ENST00000681323.1:c.793+2828G>C
ENST00000346562.6:c.2006G>C	ENSP00000319610.5:p.Gly669Ala
ENST00000356141.8:c.2102G>C	ENSP00000348460.4:p.Gly701Ala
ENST00000357798.9:c.2063G>C	ENSP00000350446.5:p.Gly688Ala
ENST00000548645.5:c.2012G>C	ENSP00000448916.1:p.Gly671Ala
ENST00000551492.5:c.2117G>C	ENSP00000450392.1:p.Gly706Ala
ENST00000551634.5:c.2024G>C	ENSP00000448373.1:p.Gly675Ala
NM_001164749.1:c.2102G>C	NP_001158221.1:p.Gly701Ala
NM_001165893.1:c.2012G>C	NP_001159365.1:p.Gly671Ala
NM_022123.2:c.2006G>C	NP_071406.1:p.Gly669Ala
NM_173159.2:c.2063G>C	NP_775182.1:p.Gly688Ala
XM_005267991.2:c.2123G>C	XP_005268048.1:p.Gly708Ala
XM_005267992.2:c.2117G>C	XP_005268049.1:p.Gly706Ala
XM_005267993.2:c.2063G>C	XP_005268050.1:p.Gly688Ala
XM_011537067.1:c.2153G>C	XP_011535369.1:p.Gly718Ala
XM_011537068.1:c.2144G>C	XP_011535370.1:p.Gly715Ala
XM_011537069.1:c.2114G>C	XP_011535371.1:p.Gly705Ala
XM_011537070.1:c.2057G>C	XP_011535372.1:p.Gly686Ala
XM_011537071.1:c.2024G>C	XP_011535373.1:p.Gly675Ala
XM_011537072.1:c.2003G>C	XP_011535374.1:p.Gly668Ala
XM_011537073.1:c.1796G>C	XP_011535375.1:p.Gly599Ala
XM_011537074.1:c.1796G>C	XP_011535376.1:p.Gly599Ala
XM_005267991.3:c.2210G>C	XP_005268048.2:p.Gly737Ala
XM_005267992.3:c.2204G>C	XP_005268049.2:p.Gly735Ala
XM_011537067.2:c.2153G>C	XP_011535369.1:p.Gly718Ala
XM_011537069.2:c.2201G>C	XP_011535371.2:p.Gly734Ala
XM_011537070.2:c.2057G>C	XP_011535372.1:p.Gly686Ala
XM_011537071.2:c.2111G>C	XP_011535373.2:p.Gly704Ala
XM_011537072.2:c.2003G>C	XP_011535374.1:p.Gly668Ala
XM_017021582.1:c.2261G>C	XP_016877071.1:p.Gly754Ala
XM_017021583.1:c.2252G>C	XP_016877072.1:p.Gly751Ala
XM_017021584.1:c.2171G>C	XP_016877073.1:p.Gly724Ala
XM_017021585.1:c.2120G>C	XP_016877074.1:p.Gly707Ala
XM_017021586.1:c.1796G>C	XP_016877075.1:p.Gly599Ala
XM_017021587.1:c.1796G>C	XP_016877076.1:p.Gly599Ala
XM_017021588.1:c.1796G>C	XP_016877077.1:p.Gly599Ala
NM_001164749.2:c.2102G>C MANE Select	NP_001158221.1:p.Gly701Ala
NM_001165893.2:c.2012G>C	NP_001159365.1:p.Gly671Ala
NM_022123.3:c.2006G>C	NP_071406.1:p.Gly669Ala
NM_173159.3:c.2063G>C	NP_775182.1:p.Gly688Ala
NM_001394988.1:c.2057G>C	NP_001381917.1:p.Gly686Ala
NM_001394989.1:c.2003G>C	NP_001381918.1:p.Gly668Ala