Canonical Allele Identifier: CA2128327713

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800544C= , CM000676.2:g.33800544C=	GRCh38
NC_000014.8:g.34269750C= , CM000676.1:g.34269750C=	GRCh37
NC_000014.7:g.33339501C=	NCBI36
NG_013036.1:g.866292C=
NG_013036.2:g.866292C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2237C= MANE Select	ENSP00000348460.4:p.Pro746=
ENST00000551634.6:c.2246C=	ENSP00000448373.2:p.Pro749=
ENST00000680362.1:c.2137C=
ENST00000681323.1:c.793+2963C=
ENST00000346562.6:c.2141C=	ENSP00000319610.5:p.Pro714=
ENST00000356141.8:c.2237C=	ENSP00000348460.4:p.Pro746=
ENST00000357798.9:c.2198C=	ENSP00000350446.5:p.Pro733=
ENST00000548645.5:c.2147C=	ENSP00000448916.1:p.Pro716=
ENST00000551492.5:c.2252C=	ENSP00000450392.1:p.Pro751=
ENST00000551634.5:c.2159C=	ENSP00000448373.1:p.Pro720=
NM_001164749.1:c.2237C=	NP_001158221.1:p.Pro746=
NM_001165893.1:c.2147C=	NP_001159365.1:p.Pro716=
NM_022123.2:c.2141C=	NP_071406.1:p.Pro714=
NM_173159.2:c.2198C=	NP_775182.1:p.Pro733=
XM_005267991.2:c.2258C=	XP_005268048.1:p.Pro753=
XM_005267992.2:c.2252C=	XP_005268049.1:p.Pro751=
XM_005267993.2:c.2198C=	XP_005268050.1:p.Pro733=
XM_011537067.1:c.2288C=	XP_011535369.1:p.Pro763=
XM_011537068.1:c.2279C=	XP_011535370.1:p.Pro760=
XM_011537069.1:c.2249C=	XP_011535371.1:p.Pro750=
XM_011537070.1:c.2192C=	XP_011535372.1:p.Pro731=
XM_011537071.1:c.2159C=	XP_011535373.1:p.Pro720=
XM_011537072.1:c.2138C=	XP_011535374.1:p.Pro713=
XM_011537073.1:c.1931C=	XP_011535375.1:p.Pro644=
XM_011537074.1:c.1931C=	XP_011535376.1:p.Pro644=
XM_005267991.3:c.2345C=	XP_005268048.2:p.Pro782=
XM_005267992.3:c.2339C=	XP_005268049.2:p.Pro780=
XM_011537067.2:c.2288C=	XP_011535369.1:p.Pro763=
XM_011537069.2:c.2336C=	XP_011535371.2:p.Pro779=
XM_011537070.2:c.2192C=	XP_011535372.1:p.Pro731=
XM_011537071.2:c.2246C=	XP_011535373.2:p.Pro749=
XM_011537072.2:c.2138C=	XP_011535374.1:p.Pro713=
XM_017021582.1:c.2396C=	XP_016877071.1:p.Pro799=
XM_017021583.1:c.2387C=	XP_016877072.1:p.Pro796=
XM_017021584.1:c.2306C=	XP_016877073.1:p.Pro769=
XM_017021585.1:c.2255C=	XP_016877074.1:p.Pro752=
XM_017021586.1:c.1931C=	XP_016877075.1:p.Pro644=
XM_017021587.1:c.1931C=	XP_016877076.1:p.Pro644=
XM_017021588.1:c.1931C=	XP_016877077.1:p.Pro644=
NM_001164749.2:c.2237C= MANE Select	NP_001158221.1:p.Pro746=
NM_001165893.2:c.2147C=	NP_001159365.1:p.Pro716=
NM_022123.3:c.2141C=	NP_071406.1:p.Pro714=
NM_173159.3:c.2198C=	NP_775182.1:p.Pro733=
NM_001394988.1:c.2192C=	NP_001381917.1:p.Pro731=
NM_001394989.1:c.2138C=	NP_001381918.1:p.Pro713=