Canonical Allele Identifier: CA389413497

Gene: NPAS3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2008A>T MANE Select	ENSP00000348460.4:p.Asn670Tyr
ENST00000551634.6:c.2017A>T	ENSP00000448373.2:p.Asn673Tyr
ENST00000680362.1:c.1908A>T
ENST00000681323.1:c.793+2734A>T
ENST00000346562.6:c.1912A>T	ENSP00000319610.5:p.Asn638Tyr
ENST00000356141.8:c.2008A>T	ENSP00000348460.4:p.Asn670Tyr
ENST00000357798.9:c.1969A>T	ENSP00000350446.5:p.Asn657Tyr
ENST00000548645.5:c.1918A>T	ENSP00000448916.1:p.Asn640Tyr
ENST00000551492.5:c.2023A>T	ENSP00000450392.1:p.Asn675Tyr
ENST00000551634.5:c.1930A>T	ENSP00000448373.1:p.Asn644Tyr
NM_001164749.1:c.2008A>T	NP_001158221.1:p.Asn670Tyr
NM_001165893.1:c.1918A>T	NP_001159365.1:p.Asn640Tyr
NM_022123.2:c.1912A>T	NP_071406.1:p.Asn638Tyr
NM_173159.2:c.1969A>T	NP_775182.1:p.Asn657Tyr
XM_005267991.2:c.2029A>T	XP_005268048.1:p.Asn677Tyr
XM_005267992.2:c.2023A>T	XP_005268049.1:p.Asn675Tyr
XM_005267993.2:c.1969A>T	XP_005268050.1:p.Asn657Tyr
XM_011537067.1:c.2059A>T	XP_011535369.1:p.Asn687Tyr
XM_011537068.1:c.2050A>T	XP_011535370.1:p.Asn684Tyr
XM_011537069.1:c.2020A>T	XP_011535371.1:p.Asn674Tyr
XM_011537070.1:c.1963A>T	XP_011535372.1:p.Asn655Tyr
XM_011537071.1:c.1930A>T	XP_011535373.1:p.Asn644Tyr
XM_011537072.1:c.1909A>T	XP_011535374.1:p.Asn637Tyr
XM_011537073.1:c.1702A>T	XP_011535375.1:p.Asn568Tyr
XM_011537074.1:c.1702A>T	XP_011535376.1:p.Asn568Tyr
XM_005267991.3:c.2116A>T	XP_005268048.2:p.Asn706Tyr
XM_005267992.3:c.2110A>T	XP_005268049.2:p.Asn704Tyr
XM_011537067.2:c.2059A>T	XP_011535369.1:p.Asn687Tyr
XM_011537069.2:c.2107A>T	XP_011535371.2:p.Asn703Tyr
XM_011537070.2:c.1963A>T	XP_011535372.1:p.Asn655Tyr
XM_011537071.2:c.2017A>T	XP_011535373.2:p.Asn673Tyr
XM_011537072.2:c.1909A>T	XP_011535374.1:p.Asn637Tyr
XM_017021582.1:c.2167A>T	XP_016877071.1:p.Asn723Tyr
XM_017021583.1:c.2158A>T	XP_016877072.1:p.Asn720Tyr
XM_017021584.1:c.2077A>T	XP_016877073.1:p.Asn693Tyr
XM_017021585.1:c.2026A>T	XP_016877074.1:p.Asn676Tyr
XM_017021586.1:c.1702A>T	XP_016877075.1:p.Asn568Tyr
XM_017021587.1:c.1702A>T	XP_016877076.1:p.Asn568Tyr
XM_017021588.1:c.1702A>T	XP_016877077.1:p.Asn568Tyr
NM_001164749.2:c.2008A>T MANE Select	NP_001158221.1:p.Asn670Tyr
NM_001165893.2:c.1918A>T	NP_001159365.1:p.Asn640Tyr
NM_022123.3:c.1912A>T	NP_071406.1:p.Asn638Tyr
NM_173159.3:c.1969A>T	NP_775182.1:p.Asn657Tyr
NM_001394988.1:c.1963A>T	NP_001381917.1:p.Asn655Tyr
NM_001394989.1:c.1909A>T	NP_001381918.1:p.Asn637Tyr