Canonical Allele Identifier: CA389413304

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269480T>G (hg19) ; chr14:g.33800274T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800274T>G , CM000676.2:g.33800274T>G	GRCh38
NC_000014.8:g.34269480T>G , CM000676.1:g.34269480T>G	GRCh37
NC_000014.7:g.33339231T>G	NCBI36
NG_013036.1:g.866022T>G
NG_013036.2:g.866022T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1967T>G MANE Select	ENSP00000348460.4:p.Ile656Ser
ENST00000551634.6:c.1976T>G	ENSP00000448373.2:p.Ile659Ser
ENST00000680362.1:c.1867T>G
ENST00000681323.1:c.793+2693T>G
ENST00000346562.6:c.1871T>G	ENSP00000319610.5:p.Ile624Ser
ENST00000356141.8:c.1967T>G	ENSP00000348460.4:p.Ile656Ser
ENST00000357798.9:c.1928T>G	ENSP00000350446.5:p.Ile643Ser
ENST00000548645.5:c.1877T>G	ENSP00000448916.1:p.Ile626Ser
ENST00000551492.5:c.1982T>G	ENSP00000450392.1:p.Ile661Ser
ENST00000551634.5:c.1889T>G	ENSP00000448373.1:p.Ile630Ser
NM_001164749.1:c.1967T>G	NP_001158221.1:p.Ile656Ser
NM_001165893.1:c.1877T>G	NP_001159365.1:p.Ile626Ser
NM_022123.2:c.1871T>G	NP_071406.1:p.Ile624Ser
NM_173159.2:c.1928T>G	NP_775182.1:p.Ile643Ser
XM_005267991.2:c.1988T>G	XP_005268048.1:p.Ile663Ser
XM_005267992.2:c.1982T>G	XP_005268049.1:p.Ile661Ser
XM_005267993.2:c.1928T>G	XP_005268050.1:p.Ile643Ser
XM_011537067.1:c.2018T>G	XP_011535369.1:p.Ile673Ser
XM_011537068.1:c.2009T>G	XP_011535370.1:p.Ile670Ser
XM_011537069.1:c.1979T>G	XP_011535371.1:p.Ile660Ser
XM_011537070.1:c.1922T>G	XP_011535372.1:p.Ile641Ser
XM_011537071.1:c.1889T>G	XP_011535373.1:p.Ile630Ser
XM_011537072.1:c.1868T>G	XP_011535374.1:p.Ile623Ser
XM_011537073.1:c.1661T>G	XP_011535375.1:p.Ile554Ser
XM_011537074.1:c.1661T>G	XP_011535376.1:p.Ile554Ser
XM_005267991.3:c.2075T>G	XP_005268048.2:p.Ile692Ser
XM_005267992.3:c.2069T>G	XP_005268049.2:p.Ile690Ser
XM_011537067.2:c.2018T>G	XP_011535369.1:p.Ile673Ser
XM_011537069.2:c.2066T>G	XP_011535371.2:p.Ile689Ser
XM_011537070.2:c.1922T>G	XP_011535372.1:p.Ile641Ser
XM_011537071.2:c.1976T>G	XP_011535373.2:p.Ile659Ser
XM_011537072.2:c.1868T>G	XP_011535374.1:p.Ile623Ser
XM_017021582.1:c.2126T>G	XP_016877071.1:p.Ile709Ser
XM_017021583.1:c.2117T>G	XP_016877072.1:p.Ile706Ser
XM_017021584.1:c.2036T>G	XP_016877073.1:p.Ile679Ser
XM_017021585.1:c.1985T>G	XP_016877074.1:p.Ile662Ser
XM_017021586.1:c.1661T>G	XP_016877075.1:p.Ile554Ser
XM_017021587.1:c.1661T>G	XP_016877076.1:p.Ile554Ser
XM_017021588.1:c.1661T>G	XP_016877077.1:p.Ile554Ser
NM_001164749.2:c.1967T>G MANE Select	NP_001158221.1:p.Ile656Ser
NM_001165893.2:c.1877T>G	NP_001159365.1:p.Ile626Ser
NM_022123.3:c.1871T>G	NP_071406.1:p.Ile624Ser
NM_173159.3:c.1928T>G	NP_775182.1:p.Ile643Ser
NM_001394988.1:c.1922T>G	NP_001381917.1:p.Ile641Ser
NM_001394989.1:c.1868T>G	NP_001381918.1:p.Ile623Ser