Canonical Allele Identifier: CA389414051

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269648C>G (hg19) ; chr14:g.33800442C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800442C>G , CM000676.2:g.33800442C>G	GRCh38
NC_000014.8:g.34269648C>G , CM000676.1:g.34269648C>G	GRCh37
NC_000014.7:g.33339399C>G	NCBI36
NG_013036.1:g.866190C>G
NG_013036.2:g.866190C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000356141.9:c.2135C>G MANE Select	ENSP00000348460.4:p.Pro712Arg
ENST00000551634.6:c.2144C>G	ENSP00000448373.2:p.Pro715Arg
ENST00000680362.1:c.2035C>G
ENST00000681323.1:c.793+2861C>G
ENST00000346562.6:c.2039C>G	ENSP00000319610.5:p.Pro680Arg
ENST00000356141.8:c.2135C>G	ENSP00000348460.4:p.Pro712Arg
ENST00000357798.9:c.2096C>G	ENSP00000350446.5:p.Pro699Arg
ENST00000548645.5:c.2045C>G	ENSP00000448916.1:p.Pro682Arg
ENST00000551492.5:c.2150C>G	ENSP00000450392.1:p.Pro717Arg
ENST00000551634.5:c.2057C>G	ENSP00000448373.1:p.Pro686Arg
NM_001164749.1:c.2135C>G	NP_001158221.1:p.Pro712Arg
NM_001165893.1:c.2045C>G	NP_001159365.1:p.Pro682Arg
NM_022123.2:c.2039C>G	NP_071406.1:p.Pro680Arg
NM_173159.2:c.2096C>G	NP_775182.1:p.Pro699Arg
XM_005267991.2:c.2156C>G	XP_005268048.1:p.Pro719Arg
XM_005267992.2:c.2150C>G	XP_005268049.1:p.Pro717Arg
XM_005267993.2:c.2096C>G	XP_005268050.1:p.Pro699Arg
XM_011537067.1:c.2186C>G	XP_011535369.1:p.Pro729Arg
XM_011537068.1:c.2177C>G	XP_011535370.1:p.Pro726Arg
XM_011537069.1:c.2147C>G	XP_011535371.1:p.Pro716Arg
XM_011537070.1:c.2090C>G	XP_011535372.1:p.Pro697Arg
XM_011537071.1:c.2057C>G	XP_011535373.1:p.Pro686Arg
XM_011537072.1:c.2036C>G	XP_011535374.1:p.Pro679Arg
XM_011537073.1:c.1829C>G	XP_011535375.1:p.Pro610Arg
XM_011537074.1:c.1829C>G	XP_011535376.1:p.Pro610Arg
XM_005267991.3:c.2243C>G	XP_005268048.2:p.Pro748Arg
XM_005267992.3:c.2237C>G	XP_005268049.2:p.Pro746Arg
XM_011537067.2:c.2186C>G	XP_011535369.1:p.Pro729Arg
XM_011537069.2:c.2234C>G	XP_011535371.2:p.Pro745Arg
XM_011537070.2:c.2090C>G	XP_011535372.1:p.Pro697Arg
XM_011537071.2:c.2144C>G	XP_011535373.2:p.Pro715Arg
XM_011537072.2:c.2036C>G	XP_011535374.1:p.Pro679Arg
XM_017021582.1:c.2294C>G	XP_016877071.1:p.Pro765Arg
XM_017021583.1:c.2285C>G	XP_016877072.1:p.Pro762Arg
XM_017021584.1:c.2204C>G	XP_016877073.1:p.Pro735Arg
XM_017021585.1:c.2153C>G	XP_016877074.1:p.Pro718Arg
XM_017021586.1:c.1829C>G	XP_016877075.1:p.Pro610Arg
XM_017021587.1:c.1829C>G	XP_016877076.1:p.Pro610Arg
XM_017021588.1:c.1829C>G	XP_016877077.1:p.Pro610Arg
NM_001164749.2:c.2135C>G MANE Select	NP_001158221.1:p.Pro712Arg
NM_001165893.2:c.2045C>G	NP_001159365.1:p.Pro682Arg
NM_022123.3:c.2039C>G	NP_071406.1:p.Pro680Arg
NM_173159.3:c.2096C>G	NP_775182.1:p.Pro699Arg
NM_001394988.1:c.2090C>G	NP_001381917.1:p.Pro697Arg
NM_001394989.1:c.2036C>G	NP_001381918.1:p.Pro679Arg