Canonical Allele Identifier: CA389413575

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269539A>G (hg19) ; chr14:g.33800333A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800333A>G , CM000676.2:g.33800333A>G	GRCh38
NC_000014.8:g.34269539A>G , CM000676.1:g.34269539A>G	GRCh37
NC_000014.7:g.33339290A>G	NCBI36
NG_013036.1:g.866081A>G
NG_013036.2:g.866081A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2026A>G MANE Select	ENSP00000348460.4:p.Asn676Asp
ENST00000551634.6:c.2035A>G	ENSP00000448373.2:p.Asn679Asp
ENST00000680362.1:c.1926A>G
ENST00000681323.1:c.793+2752A>G
ENST00000346562.6:c.1930A>G	ENSP00000319610.5:p.Asn644Asp
ENST00000356141.8:c.2026A>G	ENSP00000348460.4:p.Asn676Asp
ENST00000357798.9:c.1987A>G	ENSP00000350446.5:p.Asn663Asp
ENST00000548645.5:c.1936A>G	ENSP00000448916.1:p.Asn646Asp
ENST00000551492.5:c.2041A>G	ENSP00000450392.1:p.Asn681Asp
ENST00000551634.5:c.1948A>G	ENSP00000448373.1:p.Asn650Asp
NM_001164749.1:c.2026A>G	NP_001158221.1:p.Asn676Asp
NM_001165893.1:c.1936A>G	NP_001159365.1:p.Asn646Asp
NM_022123.2:c.1930A>G	NP_071406.1:p.Asn644Asp
NM_173159.2:c.1987A>G	NP_775182.1:p.Asn663Asp
XM_005267991.2:c.2047A>G	XP_005268048.1:p.Asn683Asp
XM_005267992.2:c.2041A>G	XP_005268049.1:p.Asn681Asp
XM_005267993.2:c.1987A>G	XP_005268050.1:p.Asn663Asp
XM_011537067.1:c.2077A>G	XP_011535369.1:p.Asn693Asp
XM_011537068.1:c.2068A>G	XP_011535370.1:p.Asn690Asp
XM_011537069.1:c.2038A>G	XP_011535371.1:p.Asn680Asp
XM_011537070.1:c.1981A>G	XP_011535372.1:p.Asn661Asp
XM_011537071.1:c.1948A>G	XP_011535373.1:p.Asn650Asp
XM_011537072.1:c.1927A>G	XP_011535374.1:p.Asn643Asp
XM_011537073.1:c.1720A>G	XP_011535375.1:p.Asn574Asp
XM_011537074.1:c.1720A>G	XP_011535376.1:p.Asn574Asp
XM_005267991.3:c.2134A>G	XP_005268048.2:p.Asn712Asp
XM_005267992.3:c.2128A>G	XP_005268049.2:p.Asn710Asp
XM_011537067.2:c.2077A>G	XP_011535369.1:p.Asn693Asp
XM_011537069.2:c.2125A>G	XP_011535371.2:p.Asn709Asp
XM_011537070.2:c.1981A>G	XP_011535372.1:p.Asn661Asp
XM_011537071.2:c.2035A>G	XP_011535373.2:p.Asn679Asp
XM_011537072.2:c.1927A>G	XP_011535374.1:p.Asn643Asp
XM_017021582.1:c.2185A>G	XP_016877071.1:p.Asn729Asp
XM_017021583.1:c.2176A>G	XP_016877072.1:p.Asn726Asp
XM_017021584.1:c.2095A>G	XP_016877073.1:p.Asn699Asp
XM_017021585.1:c.2044A>G	XP_016877074.1:p.Asn682Asp
XM_017021586.1:c.1720A>G	XP_016877075.1:p.Asn574Asp
XM_017021587.1:c.1720A>G	XP_016877076.1:p.Asn574Asp
XM_017021588.1:c.1720A>G	XP_016877077.1:p.Asn574Asp
NM_001164749.2:c.2026A>G MANE Select	NP_001158221.1:p.Asn676Asp
NM_001165893.2:c.1936A>G	NP_001159365.1:p.Asn646Asp
NM_022123.3:c.1930A>G	NP_071406.1:p.Asn644Asp
NM_173159.3:c.1987A>G	NP_775182.1:p.Asn663Asp
NM_001394988.1:c.1981A>G	NP_001381917.1:p.Asn661Asp
NM_001394989.1:c.1927A>G	NP_001381918.1:p.Asn643Asp