Canonical Allele Identifier: CA389413501

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269522A>G (hg19) ; chr14:g.33800316A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800316A>G , CM000676.2:g.33800316A>G	GRCh38
NC_000014.8:g.34269522A>G , CM000676.1:g.34269522A>G	GRCh37
NC_000014.7:g.33339273A>G	NCBI36
NG_013036.1:g.866064A>G
NG_013036.2:g.866064A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2009A>G MANE Select	ENSP00000348460.4:p.Asn670Ser
ENST00000551634.6:c.2018A>G	ENSP00000448373.2:p.Asn673Ser
ENST00000680362.1:c.1909A>G
ENST00000681323.1:c.793+2735A>G
ENST00000346562.6:c.1913A>G	ENSP00000319610.5:p.Asn638Ser
ENST00000356141.8:c.2009A>G	ENSP00000348460.4:p.Asn670Ser
ENST00000357798.9:c.1970A>G	ENSP00000350446.5:p.Asn657Ser
ENST00000548645.5:c.1919A>G	ENSP00000448916.1:p.Asn640Ser
ENST00000551492.5:c.2024A>G	ENSP00000450392.1:p.Asn675Ser
ENST00000551634.5:c.1931A>G	ENSP00000448373.1:p.Asn644Ser
NM_001164749.1:c.2009A>G	NP_001158221.1:p.Asn670Ser
NM_001165893.1:c.1919A>G	NP_001159365.1:p.Asn640Ser
NM_022123.2:c.1913A>G	NP_071406.1:p.Asn638Ser
NM_173159.2:c.1970A>G	NP_775182.1:p.Asn657Ser
XM_005267991.2:c.2030A>G	XP_005268048.1:p.Asn677Ser
XM_005267992.2:c.2024A>G	XP_005268049.1:p.Asn675Ser
XM_005267993.2:c.1970A>G	XP_005268050.1:p.Asn657Ser
XM_011537067.1:c.2060A>G	XP_011535369.1:p.Asn687Ser
XM_011537068.1:c.2051A>G	XP_011535370.1:p.Asn684Ser
XM_011537069.1:c.2021A>G	XP_011535371.1:p.Asn674Ser
XM_011537070.1:c.1964A>G	XP_011535372.1:p.Asn655Ser
XM_011537071.1:c.1931A>G	XP_011535373.1:p.Asn644Ser
XM_011537072.1:c.1910A>G	XP_011535374.1:p.Asn637Ser
XM_011537073.1:c.1703A>G	XP_011535375.1:p.Asn568Ser
XM_011537074.1:c.1703A>G	XP_011535376.1:p.Asn568Ser
XM_005267991.3:c.2117A>G	XP_005268048.2:p.Asn706Ser
XM_005267992.3:c.2111A>G	XP_005268049.2:p.Asn704Ser
XM_011537067.2:c.2060A>G	XP_011535369.1:p.Asn687Ser
XM_011537069.2:c.2108A>G	XP_011535371.2:p.Asn703Ser
XM_011537070.2:c.1964A>G	XP_011535372.1:p.Asn655Ser
XM_011537071.2:c.2018A>G	XP_011535373.2:p.Asn673Ser
XM_011537072.2:c.1910A>G	XP_011535374.1:p.Asn637Ser
XM_017021582.1:c.2168A>G	XP_016877071.1:p.Asn723Ser
XM_017021583.1:c.2159A>G	XP_016877072.1:p.Asn720Ser
XM_017021584.1:c.2078A>G	XP_016877073.1:p.Asn693Ser
XM_017021585.1:c.2027A>G	XP_016877074.1:p.Asn676Ser
XM_017021586.1:c.1703A>G	XP_016877075.1:p.Asn568Ser
XM_017021587.1:c.1703A>G	XP_016877076.1:p.Asn568Ser
XM_017021588.1:c.1703A>G	XP_016877077.1:p.Asn568Ser
NM_001164749.2:c.2009A>G MANE Select	NP_001158221.1:p.Asn670Ser
NM_001165893.2:c.1919A>G	NP_001159365.1:p.Asn640Ser
NM_022123.3:c.1913A>G	NP_071406.1:p.Asn638Ser
NM_173159.3:c.1970A>G	NP_775182.1:p.Asn657Ser
NM_001394988.1:c.1964A>G	NP_001381917.1:p.Asn655Ser
NM_001394989.1:c.1910A>G	NP_001381918.1:p.Asn637Ser