Canonical Allele Identifier: CA389413217

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269459A>T (hg19) ; chr14:g.33800253A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800253A>T , CM000676.2:g.33800253A>T	GRCh38
NC_000014.8:g.34269459A>T , CM000676.1:g.34269459A>T	GRCh37
NC_000014.7:g.33339210A>T	NCBI36
NG_013036.1:g.866001A>T
NG_013036.2:g.866001A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1946A>T MANE Select	ENSP00000348460.4:p.Lys649Met
ENST00000551634.6:c.1955A>T	ENSP00000448373.2:p.Lys652Met
ENST00000680362.1:c.1846A>T
ENST00000681323.1:c.793+2672A>T
ENST00000346562.6:c.1850A>T	ENSP00000319610.5:p.Lys617Met
ENST00000356141.8:c.1946A>T	ENSP00000348460.4:p.Lys649Met
ENST00000357798.9:c.1907A>T	ENSP00000350446.5:p.Lys636Met
ENST00000548645.5:c.1856A>T	ENSP00000448916.1:p.Lys619Met
ENST00000551492.5:c.1961A>T	ENSP00000450392.1:p.Lys654Met
ENST00000551634.5:c.1868A>T	ENSP00000448373.1:p.Lys623Met
NM_001164749.1:c.1946A>T	NP_001158221.1:p.Lys649Met
NM_001165893.1:c.1856A>T	NP_001159365.1:p.Lys619Met
NM_022123.2:c.1850A>T	NP_071406.1:p.Lys617Met
NM_173159.2:c.1907A>T	NP_775182.1:p.Lys636Met
XM_005267991.2:c.1967A>T	XP_005268048.1:p.Lys656Met
XM_005267992.2:c.1961A>T	XP_005268049.1:p.Lys654Met
XM_005267993.2:c.1907A>T	XP_005268050.1:p.Lys636Met
XM_011537067.1:c.1997A>T	XP_011535369.1:p.Lys666Met
XM_011537068.1:c.1988A>T	XP_011535370.1:p.Lys663Met
XM_011537069.1:c.1958A>T	XP_011535371.1:p.Lys653Met
XM_011537070.1:c.1901A>T	XP_011535372.1:p.Lys634Met
XM_011537071.1:c.1868A>T	XP_011535373.1:p.Lys623Met
XM_011537072.1:c.1847A>T	XP_011535374.1:p.Lys616Met
XM_011537073.1:c.1640A>T	XP_011535375.1:p.Lys547Met
XM_011537074.1:c.1640A>T	XP_011535376.1:p.Lys547Met
XM_005267991.3:c.2054A>T	XP_005268048.2:p.Lys685Met
XM_005267992.3:c.2048A>T	XP_005268049.2:p.Lys683Met
XM_011537067.2:c.1997A>T	XP_011535369.1:p.Lys666Met
XM_011537069.2:c.2045A>T	XP_011535371.2:p.Lys682Met
XM_011537070.2:c.1901A>T	XP_011535372.1:p.Lys634Met
XM_011537071.2:c.1955A>T	XP_011535373.2:p.Lys652Met
XM_011537072.2:c.1847A>T	XP_011535374.1:p.Lys616Met
XM_017021582.1:c.2105A>T	XP_016877071.1:p.Lys702Met
XM_017021583.1:c.2096A>T	XP_016877072.1:p.Lys699Met
XM_017021584.1:c.2015A>T	XP_016877073.1:p.Lys672Met
XM_017021585.1:c.1964A>T	XP_016877074.1:p.Lys655Met
XM_017021586.1:c.1640A>T	XP_016877075.1:p.Lys547Met
XM_017021587.1:c.1640A>T	XP_016877076.1:p.Lys547Met
XM_017021588.1:c.1640A>T	XP_016877077.1:p.Lys547Met
NM_001164749.2:c.1946A>T MANE Select	NP_001158221.1:p.Lys649Met
NM_001165893.2:c.1856A>T	NP_001159365.1:p.Lys619Met
NM_022123.3:c.1850A>T	NP_071406.1:p.Lys617Met
NM_173159.3:c.1907A>T	NP_775182.1:p.Lys636Met
NM_001394988.1:c.1901A>T	NP_001381917.1:p.Lys634Met
NM_001394989.1:c.1847A>T	NP_001381918.1:p.Lys616Met