Canonical Allele Identifier: CA389413409

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269501G>C (hg19) ; chr14:g.33800295G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800295G>C , CM000676.2:g.33800295G>C	GRCh38
NC_000014.8:g.34269501G>C , CM000676.1:g.34269501G>C	GRCh37
NC_000014.7:g.33339252G>C	NCBI36
NG_013036.1:g.866043G>C
NG_013036.2:g.866043G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1988G>C MANE Select	ENSP00000348460.4:p.Ser663Thr
ENST00000551634.6:c.1997G>C	ENSP00000448373.2:p.Ser666Thr
ENST00000680362.1:c.1888G>C
ENST00000681323.1:c.793+2714G>C
ENST00000346562.6:c.1892G>C	ENSP00000319610.5:p.Ser631Thr
ENST00000356141.8:c.1988G>C	ENSP00000348460.4:p.Ser663Thr
ENST00000357798.9:c.1949G>C	ENSP00000350446.5:p.Ser650Thr
ENST00000548645.5:c.1898G>C	ENSP00000448916.1:p.Ser633Thr
ENST00000551492.5:c.2003G>C	ENSP00000450392.1:p.Ser668Thr
ENST00000551634.5:c.1910G>C	ENSP00000448373.1:p.Ser637Thr
NM_001164749.1:c.1988G>C	NP_001158221.1:p.Ser663Thr
NM_001165893.1:c.1898G>C	NP_001159365.1:p.Ser633Thr
NM_022123.2:c.1892G>C	NP_071406.1:p.Ser631Thr
NM_173159.2:c.1949G>C	NP_775182.1:p.Ser650Thr
XM_005267991.2:c.2009G>C	XP_005268048.1:p.Ser670Thr
XM_005267992.2:c.2003G>C	XP_005268049.1:p.Ser668Thr
XM_005267993.2:c.1949G>C	XP_005268050.1:p.Ser650Thr
XM_011537067.1:c.2039G>C	XP_011535369.1:p.Ser680Thr
XM_011537068.1:c.2030G>C	XP_011535370.1:p.Ser677Thr
XM_011537069.1:c.2000G>C	XP_011535371.1:p.Ser667Thr
XM_011537070.1:c.1943G>C	XP_011535372.1:p.Ser648Thr
XM_011537071.1:c.1910G>C	XP_011535373.1:p.Ser637Thr
XM_011537072.1:c.1889G>C	XP_011535374.1:p.Ser630Thr
XM_011537073.1:c.1682G>C	XP_011535375.1:p.Ser561Thr
XM_011537074.1:c.1682G>C	XP_011535376.1:p.Ser561Thr
XM_005267991.3:c.2096G>C	XP_005268048.2:p.Ser699Thr
XM_005267992.3:c.2090G>C	XP_005268049.2:p.Ser697Thr
XM_011537067.2:c.2039G>C	XP_011535369.1:p.Ser680Thr
XM_011537069.2:c.2087G>C	XP_011535371.2:p.Ser696Thr
XM_011537070.2:c.1943G>C	XP_011535372.1:p.Ser648Thr
XM_011537071.2:c.1997G>C	XP_011535373.2:p.Ser666Thr
XM_011537072.2:c.1889G>C	XP_011535374.1:p.Ser630Thr
XM_017021582.1:c.2147G>C	XP_016877071.1:p.Ser716Thr
XM_017021583.1:c.2138G>C	XP_016877072.1:p.Ser713Thr
XM_017021584.1:c.2057G>C	XP_016877073.1:p.Ser686Thr
XM_017021585.1:c.2006G>C	XP_016877074.1:p.Ser669Thr
XM_017021586.1:c.1682G>C	XP_016877075.1:p.Ser561Thr
XM_017021587.1:c.1682G>C	XP_016877076.1:p.Ser561Thr
XM_017021588.1:c.1682G>C	XP_016877077.1:p.Ser561Thr
NM_001164749.2:c.1988G>C MANE Select	NP_001158221.1:p.Ser663Thr
NM_001165893.2:c.1898G>C	NP_001159365.1:p.Ser633Thr
NM_022123.3:c.1892G>C	NP_071406.1:p.Ser631Thr
NM_173159.3:c.1949G>C	NP_775182.1:p.Ser650Thr
NM_001394988.1:c.1943G>C	NP_001381917.1:p.Ser648Thr
NM_001394989.1:c.1889G>C	NP_001381918.1:p.Ser630Thr