Canonical Allele Identifier: CA389413495

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269521A>C (hg19) ; chr14:g.33800315A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800315A>C , CM000676.2:g.33800315A>C	GRCh38
NC_000014.8:g.34269521A>C , CM000676.1:g.34269521A>C	GRCh37
NC_000014.7:g.33339272A>C	NCBI36
NG_013036.1:g.866063A>C
NG_013036.2:g.866063A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2008A>C MANE Select	ENSP00000348460.4:p.Asn670His
ENST00000551634.6:c.2017A>C	ENSP00000448373.2:p.Asn673His
ENST00000680362.1:c.1908A>C
ENST00000681323.1:c.793+2734A>C
ENST00000346562.6:c.1912A>C	ENSP00000319610.5:p.Asn638His
ENST00000356141.8:c.2008A>C	ENSP00000348460.4:p.Asn670His
ENST00000357798.9:c.1969A>C	ENSP00000350446.5:p.Asn657His
ENST00000548645.5:c.1918A>C	ENSP00000448916.1:p.Asn640His
ENST00000551492.5:c.2023A>C	ENSP00000450392.1:p.Asn675His
ENST00000551634.5:c.1930A>C	ENSP00000448373.1:p.Asn644His
NM_001164749.1:c.2008A>C	NP_001158221.1:p.Asn670His
NM_001165893.1:c.1918A>C	NP_001159365.1:p.Asn640His
NM_022123.2:c.1912A>C	NP_071406.1:p.Asn638His
NM_173159.2:c.1969A>C	NP_775182.1:p.Asn657His
XM_005267991.2:c.2029A>C	XP_005268048.1:p.Asn677His
XM_005267992.2:c.2023A>C	XP_005268049.1:p.Asn675His
XM_005267993.2:c.1969A>C	XP_005268050.1:p.Asn657His
XM_011537067.1:c.2059A>C	XP_011535369.1:p.Asn687His
XM_011537068.1:c.2050A>C	XP_011535370.1:p.Asn684His
XM_011537069.1:c.2020A>C	XP_011535371.1:p.Asn674His
XM_011537070.1:c.1963A>C	XP_011535372.1:p.Asn655His
XM_011537071.1:c.1930A>C	XP_011535373.1:p.Asn644His
XM_011537072.1:c.1909A>C	XP_011535374.1:p.Asn637His
XM_011537073.1:c.1702A>C	XP_011535375.1:p.Asn568His
XM_011537074.1:c.1702A>C	XP_011535376.1:p.Asn568His
XM_005267991.3:c.2116A>C	XP_005268048.2:p.Asn706His
XM_005267992.3:c.2110A>C	XP_005268049.2:p.Asn704His
XM_011537067.2:c.2059A>C	XP_011535369.1:p.Asn687His
XM_011537069.2:c.2107A>C	XP_011535371.2:p.Asn703His
XM_011537070.2:c.1963A>C	XP_011535372.1:p.Asn655His
XM_011537071.2:c.2017A>C	XP_011535373.2:p.Asn673His
XM_011537072.2:c.1909A>C	XP_011535374.1:p.Asn637His
XM_017021582.1:c.2167A>C	XP_016877071.1:p.Asn723His
XM_017021583.1:c.2158A>C	XP_016877072.1:p.Asn720His
XM_017021584.1:c.2077A>C	XP_016877073.1:p.Asn693His
XM_017021585.1:c.2026A>C	XP_016877074.1:p.Asn676His
XM_017021586.1:c.1702A>C	XP_016877075.1:p.Asn568His
XM_017021587.1:c.1702A>C	XP_016877076.1:p.Asn568His
XM_017021588.1:c.1702A>C	XP_016877077.1:p.Asn568His
NM_001164749.2:c.2008A>C MANE Select	NP_001158221.1:p.Asn670His
NM_001165893.2:c.1918A>C	NP_001159365.1:p.Asn640His
NM_022123.3:c.1912A>C	NP_071406.1:p.Asn638His
NM_173159.3:c.1969A>C	NP_775182.1:p.Asn657His
NM_001394988.1:c.1963A>C	NP_001381917.1:p.Asn655His
NM_001394989.1:c.1909A>C	NP_001381918.1:p.Asn637His