Canonical Allele Identifier: CA389413024

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269411C>G (hg19) ; chr14:g.33800205C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800205C>G , CM000676.2:g.33800205C>G	GRCh38
NC_000014.8:g.34269411C>G , CM000676.1:g.34269411C>G	GRCh37
NC_000014.7:g.33339162C>G	NCBI36
NG_013036.1:g.865953C>G
NG_013036.2:g.865953C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1898C>G MANE Select	ENSP00000348460.4:p.Pro633Arg
ENST00000551634.6:c.1907C>G	ENSP00000448373.2:p.Pro636Arg
ENST00000680362.1:c.1798C>G
ENST00000681323.1:c.793+2624C>G
ENST00000346562.6:c.1802C>G	ENSP00000319610.5:p.Pro601Arg
ENST00000356141.8:c.1898C>G	ENSP00000348460.4:p.Pro633Arg
ENST00000357798.9:c.1859C>G	ENSP00000350446.5:p.Pro620Arg
ENST00000548645.5:c.1808C>G	ENSP00000448916.1:p.Pro603Arg
ENST00000551492.5:c.1913C>G	ENSP00000450392.1:p.Pro638Arg
ENST00000551634.5:c.1820C>G	ENSP00000448373.1:p.Pro607Arg
NM_001164749.1:c.1898C>G	NP_001158221.1:p.Pro633Arg
NM_001165893.1:c.1808C>G	NP_001159365.1:p.Pro603Arg
NM_022123.2:c.1802C>G	NP_071406.1:p.Pro601Arg
NM_173159.2:c.1859C>G	NP_775182.1:p.Pro620Arg
XM_005267991.2:c.1919C>G	XP_005268048.1:p.Pro640Arg
XM_005267992.2:c.1913C>G	XP_005268049.1:p.Pro638Arg
XM_005267993.2:c.1859C>G	XP_005268050.1:p.Pro620Arg
XM_011537067.1:c.1949C>G	XP_011535369.1:p.Pro650Arg
XM_011537068.1:c.1940C>G	XP_011535370.1:p.Pro647Arg
XM_011537069.1:c.1910C>G	XP_011535371.1:p.Pro637Arg
XM_011537070.1:c.1853C>G	XP_011535372.1:p.Pro618Arg
XM_011537071.1:c.1820C>G	XP_011535373.1:p.Pro607Arg
XM_011537072.1:c.1799C>G	XP_011535374.1:p.Pro600Arg
XM_011537073.1:c.1592C>G	XP_011535375.1:p.Pro531Arg
XM_011537074.1:c.1592C>G	XP_011535376.1:p.Pro531Arg
XM_005267991.3:c.2006C>G	XP_005268048.2:p.Pro669Arg
XM_005267992.3:c.2000C>G	XP_005268049.2:p.Pro667Arg
XM_011537067.2:c.1949C>G	XP_011535369.1:p.Pro650Arg
XM_011537069.2:c.1997C>G	XP_011535371.2:p.Pro666Arg
XM_011537070.2:c.1853C>G	XP_011535372.1:p.Pro618Arg
XM_011537071.2:c.1907C>G	XP_011535373.2:p.Pro636Arg
XM_011537072.2:c.1799C>G	XP_011535374.1:p.Pro600Arg
XM_017021582.1:c.2057C>G	XP_016877071.1:p.Pro686Arg
XM_017021583.1:c.2048C>G	XP_016877072.1:p.Pro683Arg
XM_017021584.1:c.1967C>G	XP_016877073.1:p.Pro656Arg
XM_017021585.1:c.1916C>G	XP_016877074.1:p.Pro639Arg
XM_017021586.1:c.1592C>G	XP_016877075.1:p.Pro531Arg
XM_017021587.1:c.1592C>G	XP_016877076.1:p.Pro531Arg
XM_017021588.1:c.1592C>G	XP_016877077.1:p.Pro531Arg
NM_001164749.2:c.1898C>G MANE Select	NP_001158221.1:p.Pro633Arg
NM_001165893.2:c.1808C>G	NP_001159365.1:p.Pro603Arg
NM_022123.3:c.1802C>G	NP_071406.1:p.Pro601Arg
NM_173159.3:c.1859C>G	NP_775182.1:p.Pro620Arg
NM_001394988.1:c.1853C>G	NP_001381917.1:p.Pro618Arg
NM_001394989.1:c.1799C>G	NP_001381918.1:p.Pro600Arg