Canonical Allele Identifier: CA389412933

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269389C>A (hg19) ; chr14:g.33800183C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800183C>A , CM000676.2:g.33800183C>A	GRCh38
NC_000014.8:g.34269389C>A , CM000676.1:g.34269389C>A	GRCh37
NC_000014.7:g.33339140C>A	NCBI36
NG_013036.1:g.865931C>A
NG_013036.2:g.865931C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1876C>A MANE Select	ENSP00000348460.4:p.Leu626Met
ENST00000551634.6:c.1885C>A	ENSP00000448373.2:p.Leu629Met
ENST00000680362.1:c.1776C>A
ENST00000681323.1:c.793+2602C>A
ENST00000346562.6:c.1780C>A	ENSP00000319610.5:p.Leu594Met
ENST00000356141.8:c.1876C>A	ENSP00000348460.4:p.Leu626Met
ENST00000357798.9:c.1837C>A	ENSP00000350446.5:p.Leu613Met
ENST00000548645.5:c.1786C>A	ENSP00000448916.1:p.Leu596Met
ENST00000551492.5:c.1891C>A	ENSP00000450392.1:p.Leu631Met
ENST00000551634.5:c.1798C>A	ENSP00000448373.1:p.Leu600Met
NM_001164749.1:c.1876C>A	NP_001158221.1:p.Leu626Met
NM_001165893.1:c.1786C>A	NP_001159365.1:p.Leu596Met
NM_022123.2:c.1780C>A	NP_071406.1:p.Leu594Met
NM_173159.2:c.1837C>A	NP_775182.1:p.Leu613Met
XM_005267991.2:c.1897C>A	XP_005268048.1:p.Leu633Met
XM_005267992.2:c.1891C>A	XP_005268049.1:p.Leu631Met
XM_005267993.2:c.1837C>A	XP_005268050.1:p.Leu613Met
XM_011537067.1:c.1927C>A	XP_011535369.1:p.Leu643Met
XM_011537068.1:c.1918C>A	XP_011535370.1:p.Leu640Met
XM_011537069.1:c.1888C>A	XP_011535371.1:p.Leu630Met
XM_011537070.1:c.1831C>A	XP_011535372.1:p.Leu611Met
XM_011537071.1:c.1798C>A	XP_011535373.1:p.Leu600Met
XM_011537072.1:c.1777C>A	XP_011535374.1:p.Leu593Met
XM_011537073.1:c.1570C>A	XP_011535375.1:p.Leu524Met
XM_011537074.1:c.1570C>A	XP_011535376.1:p.Leu524Met
XM_005267991.3:c.1984C>A	XP_005268048.2:p.Leu662Met
XM_005267992.3:c.1978C>A	XP_005268049.2:p.Leu660Met
XM_011537067.2:c.1927C>A	XP_011535369.1:p.Leu643Met
XM_011537069.2:c.1975C>A	XP_011535371.2:p.Leu659Met
XM_011537070.2:c.1831C>A	XP_011535372.1:p.Leu611Met
XM_011537071.2:c.1885C>A	XP_011535373.2:p.Leu629Met
XM_011537072.2:c.1777C>A	XP_011535374.1:p.Leu593Met
XM_017021582.1:c.2035C>A	XP_016877071.1:p.Leu679Met
XM_017021583.1:c.2026C>A	XP_016877072.1:p.Leu676Met
XM_017021584.1:c.1945C>A	XP_016877073.1:p.Leu649Met
XM_017021585.1:c.1894C>A	XP_016877074.1:p.Leu632Met
XM_017021586.1:c.1570C>A	XP_016877075.1:p.Leu524Met
XM_017021587.1:c.1570C>A	XP_016877076.1:p.Leu524Met
XM_017021588.1:c.1570C>A	XP_016877077.1:p.Leu524Met
NM_001164749.2:c.1876C>A MANE Select	NP_001158221.1:p.Leu626Met
NM_001165893.2:c.1786C>A	NP_001159365.1:p.Leu596Met
NM_022123.3:c.1780C>A	NP_071406.1:p.Leu594Met
NM_173159.3:c.1837C>A	NP_775182.1:p.Leu613Met
NM_001394988.1:c.1831C>A	NP_001381917.1:p.Leu611Met
NM_001394989.1:c.1777C>A	NP_001381918.1:p.Leu593Met