Canonical Allele Identifier: CA2128327290

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800345T= , CM000676.2:g.33800345T=	GRCh38
NC_000014.8:g.34269551T= , CM000676.1:g.34269551T=	GRCh37
NC_000014.7:g.33339302T=	NCBI36
NG_013036.1:g.866093T=
NG_013036.2:g.866093T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2038T= MANE Select	ENSP00000348460.4:p.Tyr680=
ENST00000551634.6:c.2047T=	ENSP00000448373.2:p.Tyr683=
ENST00000680362.1:c.1938T=
ENST00000681323.1:c.793+2764T=
ENST00000346562.6:c.1942T=	ENSP00000319610.5:p.Tyr648=
ENST00000356141.8:c.2038T=	ENSP00000348460.4:p.Tyr680=
ENST00000357798.9:c.1999T=	ENSP00000350446.5:p.Tyr667=
ENST00000548645.5:c.1948T=	ENSP00000448916.1:p.Tyr650=
ENST00000551492.5:c.2053T=	ENSP00000450392.1:p.Tyr685=
ENST00000551634.5:c.1960T=	ENSP00000448373.1:p.Tyr654=
NM_001164749.1:c.2038T=	NP_001158221.1:p.Tyr680=
NM_001165893.1:c.1948T=	NP_001159365.1:p.Tyr650=
NM_022123.2:c.1942T=	NP_071406.1:p.Tyr648=
NM_173159.2:c.1999T=	NP_775182.1:p.Tyr667=
XM_005267991.2:c.2059T=	XP_005268048.1:p.Tyr687=
XM_005267992.2:c.2053T=	XP_005268049.1:p.Tyr685=
XM_005267993.2:c.1999T=	XP_005268050.1:p.Tyr667=
XM_011537067.1:c.2089T=	XP_011535369.1:p.Tyr697=
XM_011537068.1:c.2080T=	XP_011535370.1:p.Tyr694=
XM_011537069.1:c.2050T=	XP_011535371.1:p.Tyr684=
XM_011537070.1:c.1993T=	XP_011535372.1:p.Tyr665=
XM_011537071.1:c.1960T=	XP_011535373.1:p.Tyr654=
XM_011537072.1:c.1939T=	XP_011535374.1:p.Tyr647=
XM_011537073.1:c.1732T=	XP_011535375.1:p.Tyr578=
XM_011537074.1:c.1732T=	XP_011535376.1:p.Tyr578=
XM_005267991.3:c.2146T=	XP_005268048.2:p.Tyr716=
XM_005267992.3:c.2140T=	XP_005268049.2:p.Tyr714=
XM_011537067.2:c.2089T=	XP_011535369.1:p.Tyr697=
XM_011537069.2:c.2137T=	XP_011535371.2:p.Tyr713=
XM_011537070.2:c.1993T=	XP_011535372.1:p.Tyr665=
XM_011537071.2:c.2047T=	XP_011535373.2:p.Tyr683=
XM_011537072.2:c.1939T=	XP_011535374.1:p.Tyr647=
XM_017021582.1:c.2197T=	XP_016877071.1:p.Tyr733=
XM_017021583.1:c.2188T=	XP_016877072.1:p.Tyr730=
XM_017021584.1:c.2107T=	XP_016877073.1:p.Tyr703=
XM_017021585.1:c.2056T=	XP_016877074.1:p.Tyr686=
XM_017021586.1:c.1732T=	XP_016877075.1:p.Tyr578=
XM_017021587.1:c.1732T=	XP_016877076.1:p.Tyr578=
XM_017021588.1:c.1732T=	XP_016877077.1:p.Tyr578=
NM_001164749.2:c.2038T= MANE Select	NP_001158221.1:p.Tyr680=
NM_001165893.2:c.1948T=	NP_001159365.1:p.Tyr650=
NM_022123.3:c.1942T=	NP_071406.1:p.Tyr648=
NM_173159.3:c.1999T=	NP_775182.1:p.Tyr667=
NM_001394988.1:c.1993T=	NP_001381917.1:p.Tyr665=
NM_001394989.1:c.1939T=	NP_001381918.1:p.Tyr647=