Canonical Allele Identifier: CA389413251

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269468T>G (hg19) ; chr14:g.33800262T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800262T>G , CM000676.2:g.33800262T>G	GRCh38
NC_000014.8:g.34269468T>G , CM000676.1:g.34269468T>G	GRCh37
NC_000014.7:g.33339219T>G	NCBI36
NG_013036.1:g.866010T>G
NG_013036.2:g.866010T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1955T>G MANE Select	ENSP00000348460.4:p.Ile652Ser
ENST00000551634.6:c.1964T>G	ENSP00000448373.2:p.Ile655Ser
ENST00000680362.1:c.1855T>G
ENST00000681323.1:c.793+2681T>G
ENST00000346562.6:c.1859T>G	ENSP00000319610.5:p.Ile620Ser
ENST00000356141.8:c.1955T>G	ENSP00000348460.4:p.Ile652Ser
ENST00000357798.9:c.1916T>G	ENSP00000350446.5:p.Ile639Ser
ENST00000548645.5:c.1865T>G	ENSP00000448916.1:p.Ile622Ser
ENST00000551492.5:c.1970T>G	ENSP00000450392.1:p.Ile657Ser
ENST00000551634.5:c.1877T>G	ENSP00000448373.1:p.Ile626Ser
NM_001164749.1:c.1955T>G	NP_001158221.1:p.Ile652Ser
NM_001165893.1:c.1865T>G	NP_001159365.1:p.Ile622Ser
NM_022123.2:c.1859T>G	NP_071406.1:p.Ile620Ser
NM_173159.2:c.1916T>G	NP_775182.1:p.Ile639Ser
XM_005267991.2:c.1976T>G	XP_005268048.1:p.Ile659Ser
XM_005267992.2:c.1970T>G	XP_005268049.1:p.Ile657Ser
XM_005267993.2:c.1916T>G	XP_005268050.1:p.Ile639Ser
XM_011537067.1:c.2006T>G	XP_011535369.1:p.Ile669Ser
XM_011537068.1:c.1997T>G	XP_011535370.1:p.Ile666Ser
XM_011537069.1:c.1967T>G	XP_011535371.1:p.Ile656Ser
XM_011537070.1:c.1910T>G	XP_011535372.1:p.Ile637Ser
XM_011537071.1:c.1877T>G	XP_011535373.1:p.Ile626Ser
XM_011537072.1:c.1856T>G	XP_011535374.1:p.Ile619Ser
XM_011537073.1:c.1649T>G	XP_011535375.1:p.Ile550Ser
XM_011537074.1:c.1649T>G	XP_011535376.1:p.Ile550Ser
XM_005267991.3:c.2063T>G	XP_005268048.2:p.Ile688Ser
XM_005267992.3:c.2057T>G	XP_005268049.2:p.Ile686Ser
XM_011537067.2:c.2006T>G	XP_011535369.1:p.Ile669Ser
XM_011537069.2:c.2054T>G	XP_011535371.2:p.Ile685Ser
XM_011537070.2:c.1910T>G	XP_011535372.1:p.Ile637Ser
XM_011537071.2:c.1964T>G	XP_011535373.2:p.Ile655Ser
XM_011537072.2:c.1856T>G	XP_011535374.1:p.Ile619Ser
XM_017021582.1:c.2114T>G	XP_016877071.1:p.Ile705Ser
XM_017021583.1:c.2105T>G	XP_016877072.1:p.Ile702Ser
XM_017021584.1:c.2024T>G	XP_016877073.1:p.Ile675Ser
XM_017021585.1:c.1973T>G	XP_016877074.1:p.Ile658Ser
XM_017021586.1:c.1649T>G	XP_016877075.1:p.Ile550Ser
XM_017021587.1:c.1649T>G	XP_016877076.1:p.Ile550Ser
XM_017021588.1:c.1649T>G	XP_016877077.1:p.Ile550Ser
NM_001164749.2:c.1955T>G MANE Select	NP_001158221.1:p.Ile652Ser
NM_001165893.2:c.1865T>G	NP_001159365.1:p.Ile622Ser
NM_022123.3:c.1859T>G	NP_071406.1:p.Ile620Ser
NM_173159.3:c.1916T>G	NP_775182.1:p.Ile639Ser
NM_001394988.1:c.1910T>G	NP_001381917.1:p.Ile637Ser
NM_001394989.1:c.1856T>G	NP_001381918.1:p.Ile619Ser