Canonical Allele Identifier: CA389412546

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269321G>T (hg19) ; chr14:g.33800115G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800115G>T , CM000676.2:g.33800115G>T	GRCh38
NC_000014.8:g.34269321G>T , CM000676.1:g.34269321G>T	GRCh37
NC_000014.7:g.33339072G>T	NCBI36
NG_013036.1:g.865863G>T
NG_013036.2:g.865863G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1808G>T MANE Select	ENSP00000348460.4:p.Arg603Met
ENST00000551634.6:c.1817G>T	ENSP00000448373.2:p.Arg606Met
ENST00000680362.1:c.1708G>T
ENST00000681323.1:c.793+2534G>T
ENST00000346562.6:c.1712G>T	ENSP00000319610.5:p.Arg571Met
ENST00000356141.8:c.1808G>T	ENSP00000348460.4:p.Arg603Met
ENST00000357798.9:c.1769G>T	ENSP00000350446.5:p.Arg590Met
ENST00000548645.5:c.1718G>T	ENSP00000448916.1:p.Arg573Met
ENST00000551492.5:c.1823G>T	ENSP00000450392.1:p.Arg608Met
ENST00000551634.5:c.1730G>T	ENSP00000448373.1:p.Arg577Met
NM_001164749.1:c.1808G>T	NP_001158221.1:p.Arg603Met
NM_001165893.1:c.1718G>T	NP_001159365.1:p.Arg573Met
NM_022123.2:c.1712G>T	NP_071406.1:p.Arg571Met
NM_173159.2:c.1769G>T	NP_775182.1:p.Arg590Met
XM_005267991.2:c.1829G>T	XP_005268048.1:p.Arg610Met
XM_005267992.2:c.1823G>T	XP_005268049.1:p.Arg608Met
XM_005267993.2:c.1769G>T	XP_005268050.1:p.Arg590Met
XM_011537067.1:c.1859G>T	XP_011535369.1:p.Arg620Met
XM_011537068.1:c.1850G>T	XP_011535370.1:p.Arg617Met
XM_011537069.1:c.1820G>T	XP_011535371.1:p.Arg607Met
XM_011537070.1:c.1763G>T	XP_011535372.1:p.Arg588Met
XM_011537071.1:c.1730G>T	XP_011535373.1:p.Arg577Met
XM_011537072.1:c.1709G>T	XP_011535374.1:p.Arg570Met
XM_011537073.1:c.1502G>T	XP_011535375.1:p.Arg501Met
XM_011537074.1:c.1502G>T	XP_011535376.1:p.Arg501Met
XM_005267991.3:c.1916G>T	XP_005268048.2:p.Arg639Met
XM_005267992.3:c.1910G>T	XP_005268049.2:p.Arg637Met
XM_011537067.2:c.1859G>T	XP_011535369.1:p.Arg620Met
XM_011537069.2:c.1907G>T	XP_011535371.2:p.Arg636Met
XM_011537070.2:c.1763G>T	XP_011535372.1:p.Arg588Met
XM_011537071.2:c.1817G>T	XP_011535373.2:p.Arg606Met
XM_011537072.2:c.1709G>T	XP_011535374.1:p.Arg570Met
XM_017021582.1:c.1967G>T	XP_016877071.1:p.Arg656Met
XM_017021583.1:c.1958G>T	XP_016877072.1:p.Arg653Met
XM_017021584.1:c.1877G>T	XP_016877073.1:p.Arg626Met
XM_017021585.1:c.1826G>T	XP_016877074.1:p.Arg609Met
XM_017021586.1:c.1502G>T	XP_016877075.1:p.Arg501Met
XM_017021587.1:c.1502G>T	XP_016877076.1:p.Arg501Met
XM_017021588.1:c.1502G>T	XP_016877077.1:p.Arg501Met
NM_001164749.2:c.1808G>T MANE Select	NP_001158221.1:p.Arg603Met
NM_001165893.2:c.1718G>T	NP_001159365.1:p.Arg573Met
NM_022123.3:c.1712G>T	NP_071406.1:p.Arg571Met
NM_173159.3:c.1769G>T	NP_775182.1:p.Arg590Met
NM_001394988.1:c.1763G>T	NP_001381917.1:p.Arg588Met
NM_001394989.1:c.1709G>T	NP_001381918.1:p.Arg570Met