Canonical Allele Identifier: CA7150844

Gene: NPAS3

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33799961G>C , CM000676.2:g.33799961G>C	GRCh38
NC_000014.8:g.34269167G>C , CM000676.1:g.34269167G>C	GRCh37
NC_000014.7:g.33338918G>C	NCBI36
NG_013036.1:g.865709G>C
NG_013036.2:g.865709G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1654G>C MANE Select	ENSP00000348460.4:p.Ala552Pro
ENST00000551634.6:c.1663G>C	ENSP00000448373.2:p.Ala555Pro
ENST00000680362.1:c.1554G>C
ENST00000681323.1:c.793+2380G>C
ENST00000346562.6:c.1558G>C	ENSP00000319610.5:p.Ala520Pro
ENST00000356141.8:c.1654G>C	ENSP00000348460.4:p.Ala552Pro
ENST00000357798.9:c.1615G>C	ENSP00000350446.5:p.Ala539Pro
ENST00000548645.5:c.1564G>C	ENSP00000448916.1:p.Ala522Pro
ENST00000551492.5:c.1669G>C	ENSP00000450392.1:p.Ala557Pro
ENST00000551634.5:c.1576G>C	ENSP00000448373.1:p.Ala526Pro
NM_001164749.1:c.1654G>C	NP_001158221.1:p.Ala552Pro
NM_001165893.1:c.1564G>C	NP_001159365.1:p.Ala522Pro
NM_022123.2:c.1558G>C	NP_071406.1:p.Ala520Pro
NM_173159.2:c.1615G>C	NP_775182.1:p.Ala539Pro
XM_005267991.2:c.1675G>C	XP_005268048.1:p.Ala559Pro
XM_005267992.2:c.1669G>C	XP_005268049.1:p.Ala557Pro
XM_005267993.2:c.1615G>C	XP_005268050.1:p.Ala539Pro
XM_011537067.1:c.1705G>C	XP_011535369.1:p.Ala569Pro
XM_011537068.1:c.1696G>C	XP_011535370.1:p.Ala566Pro
XM_011537069.1:c.1666G>C	XP_011535371.1:p.Ala556Pro
XM_011537070.1:c.1609G>C	XP_011535372.1:p.Ala537Pro
XM_011537071.1:c.1576G>C	XP_011535373.1:p.Ala526Pro
XM_011537072.1:c.1555G>C	XP_011535374.1:p.Ala519Pro
XM_011537073.1:c.1348G>C	XP_011535375.1:p.Ala450Pro
XM_011537074.1:c.1348G>C	XP_011535376.1:p.Ala450Pro
XM_005267991.3:c.1762G>C	XP_005268048.2:p.Ala588Pro
XM_005267992.3:c.1756G>C	XP_005268049.2:p.Ala586Pro
XM_011537067.2:c.1705G>C	XP_011535369.1:p.Ala569Pro
XM_011537069.2:c.1753G>C	XP_011535371.2:p.Ala585Pro
XM_011537070.2:c.1609G>C	XP_011535372.1:p.Ala537Pro
XM_011537071.2:c.1663G>C	XP_011535373.2:p.Ala555Pro
XM_011537072.2:c.1555G>C	XP_011535374.1:p.Ala519Pro
XM_017021582.1:c.1813G>C	XP_016877071.1:p.Ala605Pro
XM_017021583.1:c.1804G>C	XP_016877072.1:p.Ala602Pro
XM_017021584.1:c.1723G>C	XP_016877073.1:p.Ala575Pro
XM_017021585.1:c.1672G>C	XP_016877074.1:p.Ala558Pro
XM_017021586.1:c.1348G>C	XP_016877075.1:p.Ala450Pro
XM_017021587.1:c.1348G>C	XP_016877076.1:p.Ala450Pro
XM_017021588.1:c.1348G>C	XP_016877077.1:p.Ala450Pro
NM_001164749.2:c.1654G>C MANE Select	NP_001158221.1:p.Ala552Pro
NM_001165893.2:c.1564G>C	NP_001159365.1:p.Ala522Pro
NM_022123.3:c.1558G>C	NP_071406.1:p.Ala520Pro
NM_173159.3:c.1615G>C	NP_775182.1:p.Ala539Pro
NM_001394988.1:c.1609G>C	NP_001381917.1:p.Ala537Pro
NM_001394989.1:c.1555G>C	NP_001381918.1:p.Ala519Pro