Canonical Allele Identifier: CA389413108

Gene: NPAS3

Linked Data

• gnomAD v4: 14-33800229-A-T
• MyVariant Identifiers: chr14:g.34269435A>T (hg19) ; chr14:g.33800229A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800229A>T , CM000676.2:g.33800229A>T	GRCh38
NC_000014.8:g.34269435A>T , CM000676.1:g.34269435A>T	GRCh37
NC_000014.7:g.33339186A>T	NCBI36
NG_013036.1:g.865977A>T
NG_013036.2:g.865977A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1922A>T MANE Select	ENSP00000348460.4:p.Asn641Ile
ENST00000551634.6:c.1931A>T	ENSP00000448373.2:p.Asn644Ile
ENST00000680362.1:c.1822A>T
ENST00000681323.1:c.793+2648A>T
ENST00000346562.6:c.1826A>T	ENSP00000319610.5:p.Asn609Ile
ENST00000356141.8:c.1922A>T	ENSP00000348460.4:p.Asn641Ile
ENST00000357798.9:c.1883A>T	ENSP00000350446.5:p.Asn628Ile
ENST00000548645.5:c.1832A>T	ENSP00000448916.1:p.Asn611Ile
ENST00000551492.5:c.1937A>T	ENSP00000450392.1:p.Asn646Ile
ENST00000551634.5:c.1844A>T	ENSP00000448373.1:p.Asn615Ile
NM_001164749.1:c.1922A>T	NP_001158221.1:p.Asn641Ile
NM_001165893.1:c.1832A>T	NP_001159365.1:p.Asn611Ile
NM_022123.2:c.1826A>T	NP_071406.1:p.Asn609Ile
NM_173159.2:c.1883A>T	NP_775182.1:p.Asn628Ile
XM_005267991.2:c.1943A>T	XP_005268048.1:p.Asn648Ile
XM_005267992.2:c.1937A>T	XP_005268049.1:p.Asn646Ile
XM_005267993.2:c.1883A>T	XP_005268050.1:p.Asn628Ile
XM_011537067.1:c.1973A>T	XP_011535369.1:p.Asn658Ile
XM_011537068.1:c.1964A>T	XP_011535370.1:p.Asn655Ile
XM_011537069.1:c.1934A>T	XP_011535371.1:p.Asn645Ile
XM_011537070.1:c.1877A>T	XP_011535372.1:p.Asn626Ile
XM_011537071.1:c.1844A>T	XP_011535373.1:p.Asn615Ile
XM_011537072.1:c.1823A>T	XP_011535374.1:p.Asn608Ile
XM_011537073.1:c.1616A>T	XP_011535375.1:p.Asn539Ile
XM_011537074.1:c.1616A>T	XP_011535376.1:p.Asn539Ile
XM_005267991.3:c.2030A>T	XP_005268048.2:p.Asn677Ile
XM_005267992.3:c.2024A>T	XP_005268049.2:p.Asn675Ile
XM_011537067.2:c.1973A>T	XP_011535369.1:p.Asn658Ile
XM_011537069.2:c.2021A>T	XP_011535371.2:p.Asn674Ile
XM_011537070.2:c.1877A>T	XP_011535372.1:p.Asn626Ile
XM_011537071.2:c.1931A>T	XP_011535373.2:p.Asn644Ile
XM_011537072.2:c.1823A>T	XP_011535374.1:p.Asn608Ile
XM_017021582.1:c.2081A>T	XP_016877071.1:p.Asn694Ile
XM_017021583.1:c.2072A>T	XP_016877072.1:p.Asn691Ile
XM_017021584.1:c.1991A>T	XP_016877073.1:p.Asn664Ile
XM_017021585.1:c.1940A>T	XP_016877074.1:p.Asn647Ile
XM_017021586.1:c.1616A>T	XP_016877075.1:p.Asn539Ile
XM_017021587.1:c.1616A>T	XP_016877076.1:p.Asn539Ile
XM_017021588.1:c.1616A>T	XP_016877077.1:p.Asn539Ile
NM_001164749.2:c.1922A>T MANE Select	NP_001158221.1:p.Asn641Ile
NM_001165893.2:c.1832A>T	NP_001159365.1:p.Asn611Ile
NM_022123.3:c.1826A>T	NP_071406.1:p.Asn609Ile
NM_173159.3:c.1883A>T	NP_775182.1:p.Asn628Ile
NM_001394988.1:c.1877A>T	NP_001381917.1:p.Asn626Ile
NM_001394989.1:c.1823A>T	NP_001381918.1:p.Asn608Ile