Canonical Allele Identifier: CA389412406

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269302C>G (hg19) ; chr14:g.33800096C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800096C>G , CM000676.2:g.33800096C>G	GRCh38
NC_000014.8:g.34269302C>G , CM000676.1:g.34269302C>G	GRCh37
NC_000014.7:g.33339053C>G	NCBI36
NG_013036.1:g.865844C>G
NG_013036.2:g.865844C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1789C>G MANE Select	ENSP00000348460.4:p.His597Asp
ENST00000551634.6:c.1798C>G	ENSP00000448373.2:p.His600Asp
ENST00000680362.1:c.1689C>G
ENST00000681323.1:c.793+2515C>G
ENST00000346562.6:c.1693C>G	ENSP00000319610.5:p.His565Asp
ENST00000356141.8:c.1789C>G	ENSP00000348460.4:p.His597Asp
ENST00000357798.9:c.1750C>G	ENSP00000350446.5:p.His584Asp
ENST00000548645.5:c.1699C>G	ENSP00000448916.1:p.His567Asp
ENST00000551492.5:c.1804C>G	ENSP00000450392.1:p.His602Asp
ENST00000551634.5:c.1711C>G	ENSP00000448373.1:p.His571Asp
NM_001164749.1:c.1789C>G	NP_001158221.1:p.His597Asp
NM_001165893.1:c.1699C>G	NP_001159365.1:p.His567Asp
NM_022123.2:c.1693C>G	NP_071406.1:p.His565Asp
NM_173159.2:c.1750C>G	NP_775182.1:p.His584Asp
XM_005267991.2:c.1810C>G	XP_005268048.1:p.His604Asp
XM_005267992.2:c.1804C>G	XP_005268049.1:p.His602Asp
XM_005267993.2:c.1750C>G	XP_005268050.1:p.His584Asp
XM_011537067.1:c.1840C>G	XP_011535369.1:p.His614Asp
XM_011537068.1:c.1831C>G	XP_011535370.1:p.His611Asp
XM_011537069.1:c.1801C>G	XP_011535371.1:p.His601Asp
XM_011537070.1:c.1744C>G	XP_011535372.1:p.His582Asp
XM_011537071.1:c.1711C>G	XP_011535373.1:p.His571Asp
XM_011537072.1:c.1690C>G	XP_011535374.1:p.His564Asp
XM_011537073.1:c.1483C>G	XP_011535375.1:p.His495Asp
XM_011537074.1:c.1483C>G	XP_011535376.1:p.His495Asp
XM_005267991.3:c.1897C>G	XP_005268048.2:p.His633Asp
XM_005267992.3:c.1891C>G	XP_005268049.2:p.His631Asp
XM_011537067.2:c.1840C>G	XP_011535369.1:p.His614Asp
XM_011537069.2:c.1888C>G	XP_011535371.2:p.His630Asp
XM_011537070.2:c.1744C>G	XP_011535372.1:p.His582Asp
XM_011537071.2:c.1798C>G	XP_011535373.2:p.His600Asp
XM_011537072.2:c.1690C>G	XP_011535374.1:p.His564Asp
XM_017021582.1:c.1948C>G	XP_016877071.1:p.His650Asp
XM_017021583.1:c.1939C>G	XP_016877072.1:p.His647Asp
XM_017021584.1:c.1858C>G	XP_016877073.1:p.His620Asp
XM_017021585.1:c.1807C>G	XP_016877074.1:p.His603Asp
XM_017021586.1:c.1483C>G	XP_016877075.1:p.His495Asp
XM_017021587.1:c.1483C>G	XP_016877076.1:p.His495Asp
XM_017021588.1:c.1483C>G	XP_016877077.1:p.His495Asp
NM_001164749.2:c.1789C>G MANE Select	NP_001158221.1:p.His597Asp
NM_001165893.2:c.1699C>G	NP_001159365.1:p.His567Asp
NM_022123.3:c.1693C>G	NP_071406.1:p.His565Asp
NM_173159.3:c.1750C>G	NP_775182.1:p.His584Asp
NM_001394988.1:c.1744C>G	NP_001381917.1:p.His582Asp
NM_001394989.1:c.1690C>G	NP_001381918.1:p.His564Asp