Canonical Allele Identifier: CA389414332

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269785A>T (hg19) ; chr14:g.33800579A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800579A>T , CM000676.2:g.33800579A>T	GRCh38
NC_000014.8:g.34269785A>T , CM000676.1:g.34269785A>T	GRCh37
NC_000014.7:g.33339536A>T	NCBI36
NG_013036.1:g.866327A>T
NG_013036.2:g.866327A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2272A>T MANE Select	ENSP00000348460.4:p.Lys758Ter
ENST00000551634.6:c.2281A>T	ENSP00000448373.2:p.Lys761Ter
ENST00000680362.1:c.2172A>T
ENST00000681323.1:c.793+2998A>T
ENST00000346562.6:c.2176A>T	ENSP00000319610.5:p.Lys726Ter
ENST00000356141.8:c.2272A>T	ENSP00000348460.4:p.Lys758Ter
ENST00000357798.9:c.2233A>T	ENSP00000350446.5:p.Lys745Ter
ENST00000548645.5:c.2182A>T	ENSP00000448916.1:p.Lys728Ter
ENST00000551492.5:c.2287A>T	ENSP00000450392.1:p.Lys763Ter
ENST00000551634.5:c.2194A>T	ENSP00000448373.1:p.Lys732Ter
NM_001164749.1:c.2272A>T	NP_001158221.1:p.Lys758Ter
NM_001165893.1:c.2182A>T	NP_001159365.1:p.Lys728Ter
NM_022123.2:c.2176A>T	NP_071406.1:p.Lys726Ter
NM_173159.2:c.2233A>T	NP_775182.1:p.Lys745Ter
XM_005267991.2:c.2293A>T	XP_005268048.1:p.Lys765Ter
XM_005267992.2:c.2287A>T	XP_005268049.1:p.Lys763Ter
XM_005267993.2:c.2233A>T	XP_005268050.1:p.Lys745Ter
XM_011537067.1:c.2323A>T	XP_011535369.1:p.Lys775Ter
XM_011537068.1:c.2314A>T	XP_011535370.1:p.Lys772Ter
XM_011537069.1:c.2284A>T	XP_011535371.1:p.Lys762Ter
XM_011537070.1:c.2227A>T	XP_011535372.1:p.Lys743Ter
XM_011537071.1:c.2194A>T	XP_011535373.1:p.Lys732Ter
XM_011537072.1:c.2173A>T	XP_011535374.1:p.Lys725Ter
XM_011537073.1:c.1966A>T	XP_011535375.1:p.Lys656Ter
XM_011537074.1:c.1966A>T	XP_011535376.1:p.Lys656Ter
XM_005267991.3:c.2380A>T	XP_005268048.2:p.Lys794Ter
XM_005267992.3:c.2374A>T	XP_005268049.2:p.Lys792Ter
XM_011537067.2:c.2323A>T	XP_011535369.1:p.Lys775Ter
XM_011537069.2:c.2371A>T	XP_011535371.2:p.Lys791Ter
XM_011537070.2:c.2227A>T	XP_011535372.1:p.Lys743Ter
XM_011537071.2:c.2281A>T	XP_011535373.2:p.Lys761Ter
XM_011537072.2:c.2173A>T	XP_011535374.1:p.Lys725Ter
XM_017021582.1:c.2431A>T	XP_016877071.1:p.Lys811Ter
XM_017021583.1:c.2422A>T	XP_016877072.1:p.Lys808Ter
XM_017021584.1:c.2341A>T	XP_016877073.1:p.Lys781Ter
XM_017021585.1:c.2290A>T	XP_016877074.1:p.Lys764Ter
XM_017021586.1:c.1966A>T	XP_016877075.1:p.Lys656Ter
XM_017021587.1:c.1966A>T	XP_016877076.1:p.Lys656Ter
XM_017021588.1:c.1966A>T	XP_016877077.1:p.Lys656Ter
NM_001164749.2:c.2272A>T MANE Select	NP_001158221.1:p.Lys758Ter
NM_001165893.2:c.2182A>T	NP_001159365.1:p.Lys728Ter
NM_022123.3:c.2176A>T	NP_071406.1:p.Lys726Ter
NM_173159.3:c.2233A>T	NP_775182.1:p.Lys745Ter
NM_001394988.1:c.2227A>T	NP_001381917.1:p.Lys743Ter
NM_001394989.1:c.2173A>T	NP_001381918.1:p.Lys725Ter