Canonical Allele Identifier: CA486092985

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269472A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800266A>C , CM000676.2:g.33800266A>C	GRCh38
NC_000014.8:g.34269472A>C , CM000676.1:g.34269472A>C	GRCh37
NC_000014.7:g.33339223A>C	NCBI36
NG_013036.1:g.866014A>C
NG_013036.2:g.866014A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1959A>C MANE Select	ENSP00000348460.4:p.Ser653=
ENST00000551634.6:c.1968A>C	ENSP00000448373.2:p.Ser656=
ENST00000680362.1:c.1859A>C
ENST00000681323.1:c.793+2685A>C
ENST00000346562.6:c.1863A>C	ENSP00000319610.5:p.Ser621=
ENST00000356141.8:c.1959A>C	ENSP00000348460.4:p.Ser653=
ENST00000357798.9:c.1920A>C	ENSP00000350446.5:p.Ser640=
ENST00000548645.5:c.1869A>C	ENSP00000448916.1:p.Ser623=
ENST00000551492.5:c.1974A>C	ENSP00000450392.1:p.Ser658=
ENST00000551634.5:c.1881A>C	ENSP00000448373.1:p.Ser627=
NM_001164749.1:c.1959A>C	NP_001158221.1:p.Ser653=
NM_001165893.1:c.1869A>C	NP_001159365.1:p.Ser623=
NM_022123.2:c.1863A>C	NP_071406.1:p.Ser621=
NM_173159.2:c.1920A>C	NP_775182.1:p.Ser640=
XM_005267991.2:c.1980A>C	XP_005268048.1:p.Ser660=
XM_005267992.2:c.1974A>C	XP_005268049.1:p.Ser658=
XM_005267993.2:c.1920A>C	XP_005268050.1:p.Ser640=
XM_011537067.1:c.2010A>C	XP_011535369.1:p.Ser670=
XM_011537068.1:c.2001A>C	XP_011535370.1:p.Ser667=
XM_011537069.1:c.1971A>C	XP_011535371.1:p.Ser657=
XM_011537070.1:c.1914A>C	XP_011535372.1:p.Ser638=
XM_011537071.1:c.1881A>C	XP_011535373.1:p.Ser627=
XM_011537072.1:c.1860A>C	XP_011535374.1:p.Ser620=
XM_011537073.1:c.1653A>C	XP_011535375.1:p.Ser551=
XM_011537074.1:c.1653A>C	XP_011535376.1:p.Ser551=
XM_005267991.3:c.2067A>C	XP_005268048.2:p.Ser689=
XM_005267992.3:c.2061A>C	XP_005268049.2:p.Ser687=
XM_011537067.2:c.2010A>C	XP_011535369.1:p.Ser670=
XM_011537069.2:c.2058A>C	XP_011535371.2:p.Ser686=
XM_011537070.2:c.1914A>C	XP_011535372.1:p.Ser638=
XM_011537071.2:c.1968A>C	XP_011535373.2:p.Ser656=
XM_011537072.2:c.1860A>C	XP_011535374.1:p.Ser620=
XM_017021582.1:c.2118A>C	XP_016877071.1:p.Ser706=
XM_017021583.1:c.2109A>C	XP_016877072.1:p.Ser703=
XM_017021584.1:c.2028A>C	XP_016877073.1:p.Ser676=
XM_017021585.1:c.1977A>C	XP_016877074.1:p.Ser659=
XM_017021586.1:c.1653A>C	XP_016877075.1:p.Ser551=
XM_017021587.1:c.1653A>C	XP_016877076.1:p.Ser551=
XM_017021588.1:c.1653A>C	XP_016877077.1:p.Ser551=
NM_001164749.2:c.1959A>C MANE Select	NP_001158221.1:p.Ser653=
NM_001165893.2:c.1869A>C	NP_001159365.1:p.Ser623=
NM_022123.3:c.1863A>C	NP_071406.1:p.Ser621=
NM_173159.3:c.1920A>C	NP_775182.1:p.Ser640=
NM_001394988.1:c.1914A>C	NP_001381917.1:p.Ser638=
NM_001394989.1:c.1860A>C	NP_001381918.1:p.Ser620=