Canonical Allele Identifier: CA389413527

Gene: NPAS3

Linked Data

• dbSNP Id: rs1404401727
• MyVariant Identifiers: chr14:g.34269529G>C (hg19) ; chr14:g.33800323G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800323G>C , CM000676.2:g.33800323G>C	GRCh38
NC_000014.8:g.34269529G>C , CM000676.1:g.34269529G>C	GRCh37
NC_000014.7:g.33339280G>C	NCBI36
NG_013036.1:g.866071G>C
NG_013036.2:g.866071G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2016G>C MANE Select	ENSP00000348460.4:p.Glu672Asp
ENST00000551634.6:c.2025G>C	ENSP00000448373.2:p.Glu675Asp
ENST00000680362.1:c.1916G>C
ENST00000681323.1:c.793+2742G>C
ENST00000346562.6:c.1920G>C	ENSP00000319610.5:p.Glu640Asp
ENST00000356141.8:c.2016G>C	ENSP00000348460.4:p.Glu672Asp
ENST00000357798.9:c.1977G>C	ENSP00000350446.5:p.Glu659Asp
ENST00000548645.5:c.1926G>C	ENSP00000448916.1:p.Glu642Asp
ENST00000551492.5:c.2031G>C	ENSP00000450392.1:p.Glu677Asp
ENST00000551634.5:c.1938G>C	ENSP00000448373.1:p.Glu646Asp
NM_001164749.1:c.2016G>C	NP_001158221.1:p.Glu672Asp
NM_001165893.1:c.1926G>C	NP_001159365.1:p.Glu642Asp
NM_022123.2:c.1920G>C	NP_071406.1:p.Glu640Asp
NM_173159.2:c.1977G>C	NP_775182.1:p.Glu659Asp
XM_005267991.2:c.2037G>C	XP_005268048.1:p.Glu679Asp
XM_005267992.2:c.2031G>C	XP_005268049.1:p.Glu677Asp
XM_005267993.2:c.1977G>C	XP_005268050.1:p.Glu659Asp
XM_011537067.1:c.2067G>C	XP_011535369.1:p.Glu689Asp
XM_011537068.1:c.2058G>C	XP_011535370.1:p.Glu686Asp
XM_011537069.1:c.2028G>C	XP_011535371.1:p.Glu676Asp
XM_011537070.1:c.1971G>C	XP_011535372.1:p.Glu657Asp
XM_011537071.1:c.1938G>C	XP_011535373.1:p.Glu646Asp
XM_011537072.1:c.1917G>C	XP_011535374.1:p.Glu639Asp
XM_011537073.1:c.1710G>C	XP_011535375.1:p.Glu570Asp
XM_011537074.1:c.1710G>C	XP_011535376.1:p.Glu570Asp
XM_005267991.3:c.2124G>C	XP_005268048.2:p.Glu708Asp
XM_005267992.3:c.2118G>C	XP_005268049.2:p.Glu706Asp
XM_011537067.2:c.2067G>C	XP_011535369.1:p.Glu689Asp
XM_011537069.2:c.2115G>C	XP_011535371.2:p.Glu705Asp
XM_011537070.2:c.1971G>C	XP_011535372.1:p.Glu657Asp
XM_011537071.2:c.2025G>C	XP_011535373.2:p.Glu675Asp
XM_011537072.2:c.1917G>C	XP_011535374.1:p.Glu639Asp
XM_017021582.1:c.2175G>C	XP_016877071.1:p.Glu725Asp
XM_017021583.1:c.2166G>C	XP_016877072.1:p.Glu722Asp
XM_017021584.1:c.2085G>C	XP_016877073.1:p.Glu695Asp
XM_017021585.1:c.2034G>C	XP_016877074.1:p.Glu678Asp
XM_017021586.1:c.1710G>C	XP_016877075.1:p.Glu570Asp
XM_017021587.1:c.1710G>C	XP_016877076.1:p.Glu570Asp
XM_017021588.1:c.1710G>C	XP_016877077.1:p.Glu570Asp
NM_001164749.2:c.2016G>C MANE Select	NP_001158221.1:p.Glu672Asp
NM_001165893.2:c.1926G>C	NP_001159365.1:p.Glu642Asp
NM_022123.3:c.1920G>C	NP_071406.1:p.Glu640Asp
NM_173159.3:c.1977G>C	NP_775182.1:p.Glu659Asp
NM_001394988.1:c.1971G>C	NP_001381917.1:p.Glu657Asp
NM_001394989.1:c.1917G>C	NP_001381918.1:p.Glu639Asp