Canonical Allele Identifier: CA389413965

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269627G>T (hg19) ; chr14:g.33800421G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800421G>T , CM000676.2:g.33800421G>T	GRCh38
NC_000014.8:g.34269627G>T , CM000676.1:g.34269627G>T	GRCh37
NC_000014.7:g.33339378G>T	NCBI36
NG_013036.1:g.866169G>T
NG_013036.2:g.866169G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2114G>T MANE Select	ENSP00000348460.4:p.Gly705Val
ENST00000551634.6:c.2123G>T	ENSP00000448373.2:p.Gly708Val
ENST00000680362.1:c.2014G>T
ENST00000681323.1:c.793+2840G>T
ENST00000346562.6:c.2018G>T	ENSP00000319610.5:p.Gly673Val
ENST00000356141.8:c.2114G>T	ENSP00000348460.4:p.Gly705Val
ENST00000357798.9:c.2075G>T	ENSP00000350446.5:p.Gly692Val
ENST00000548645.5:c.2024G>T	ENSP00000448916.1:p.Gly675Val
ENST00000551492.5:c.2129G>T	ENSP00000450392.1:p.Gly710Val
ENST00000551634.5:c.2036G>T	ENSP00000448373.1:p.Gly679Val
NM_001164749.1:c.2114G>T	NP_001158221.1:p.Gly705Val
NM_001165893.1:c.2024G>T	NP_001159365.1:p.Gly675Val
NM_022123.2:c.2018G>T	NP_071406.1:p.Gly673Val
NM_173159.2:c.2075G>T	NP_775182.1:p.Gly692Val
XM_005267991.2:c.2135G>T	XP_005268048.1:p.Gly712Val
XM_005267992.2:c.2129G>T	XP_005268049.1:p.Gly710Val
XM_005267993.2:c.2075G>T	XP_005268050.1:p.Gly692Val
XM_011537067.1:c.2165G>T	XP_011535369.1:p.Gly722Val
XM_011537068.1:c.2156G>T	XP_011535370.1:p.Gly719Val
XM_011537069.1:c.2126G>T	XP_011535371.1:p.Gly709Val
XM_011537070.1:c.2069G>T	XP_011535372.1:p.Gly690Val
XM_011537071.1:c.2036G>T	XP_011535373.1:p.Gly679Val
XM_011537072.1:c.2015G>T	XP_011535374.1:p.Gly672Val
XM_011537073.1:c.1808G>T	XP_011535375.1:p.Gly603Val
XM_011537074.1:c.1808G>T	XP_011535376.1:p.Gly603Val
XM_005267991.3:c.2222G>T	XP_005268048.2:p.Gly741Val
XM_005267992.3:c.2216G>T	XP_005268049.2:p.Gly739Val
XM_011537067.2:c.2165G>T	XP_011535369.1:p.Gly722Val
XM_011537069.2:c.2213G>T	XP_011535371.2:p.Gly738Val
XM_011537070.2:c.2069G>T	XP_011535372.1:p.Gly690Val
XM_011537071.2:c.2123G>T	XP_011535373.2:p.Gly708Val
XM_011537072.2:c.2015G>T	XP_011535374.1:p.Gly672Val
XM_017021582.1:c.2273G>T	XP_016877071.1:p.Gly758Val
XM_017021583.1:c.2264G>T	XP_016877072.1:p.Gly755Val
XM_017021584.1:c.2183G>T	XP_016877073.1:p.Gly728Val
XM_017021585.1:c.2132G>T	XP_016877074.1:p.Gly711Val
XM_017021586.1:c.1808G>T	XP_016877075.1:p.Gly603Val
XM_017021587.1:c.1808G>T	XP_016877076.1:p.Gly603Val
XM_017021588.1:c.1808G>T	XP_016877077.1:p.Gly603Val
NM_001164749.2:c.2114G>T MANE Select	NP_001158221.1:p.Gly705Val
NM_001165893.2:c.2024G>T	NP_001159365.1:p.Gly675Val
NM_022123.3:c.2018G>T	NP_071406.1:p.Gly673Val
NM_173159.3:c.2075G>T	NP_775182.1:p.Gly692Val
NM_001394988.1:c.2069G>T	NP_001381917.1:p.Gly690Val
NM_001394989.1:c.2015G>T	NP_001381918.1:p.Gly672Val