Canonical Allele Identifier: CA389413321

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269483A>T (hg19) ; chr14:g.33800277A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800277A>T , CM000676.2:g.33800277A>T	GRCh38
NC_000014.8:g.34269483A>T , CM000676.1:g.34269483A>T	GRCh37
NC_000014.7:g.33339234A>T	NCBI36
NG_013036.1:g.866025A>T
NG_013036.2:g.866025A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1970A>T MANE Select	ENSP00000348460.4:p.Asn657Ile
ENST00000551634.6:c.1979A>T	ENSP00000448373.2:p.Asn660Ile
ENST00000680362.1:c.1870A>T
ENST00000681323.1:c.793+2696A>T
ENST00000346562.6:c.1874A>T	ENSP00000319610.5:p.Asn625Ile
ENST00000356141.8:c.1970A>T	ENSP00000348460.4:p.Asn657Ile
ENST00000357798.9:c.1931A>T	ENSP00000350446.5:p.Asn644Ile
ENST00000548645.5:c.1880A>T	ENSP00000448916.1:p.Asn627Ile
ENST00000551492.5:c.1985A>T	ENSP00000450392.1:p.Asn662Ile
ENST00000551634.5:c.1892A>T	ENSP00000448373.1:p.Asn631Ile
NM_001164749.1:c.1970A>T	NP_001158221.1:p.Asn657Ile
NM_001165893.1:c.1880A>T	NP_001159365.1:p.Asn627Ile
NM_022123.2:c.1874A>T	NP_071406.1:p.Asn625Ile
NM_173159.2:c.1931A>T	NP_775182.1:p.Asn644Ile
XM_005267991.2:c.1991A>T	XP_005268048.1:p.Asn664Ile
XM_005267992.2:c.1985A>T	XP_005268049.1:p.Asn662Ile
XM_005267993.2:c.1931A>T	XP_005268050.1:p.Asn644Ile
XM_011537067.1:c.2021A>T	XP_011535369.1:p.Asn674Ile
XM_011537068.1:c.2012A>T	XP_011535370.1:p.Asn671Ile
XM_011537069.1:c.1982A>T	XP_011535371.1:p.Asn661Ile
XM_011537070.1:c.1925A>T	XP_011535372.1:p.Asn642Ile
XM_011537071.1:c.1892A>T	XP_011535373.1:p.Asn631Ile
XM_011537072.1:c.1871A>T	XP_011535374.1:p.Asn624Ile
XM_011537073.1:c.1664A>T	XP_011535375.1:p.Asn555Ile
XM_011537074.1:c.1664A>T	XP_011535376.1:p.Asn555Ile
XM_005267991.3:c.2078A>T	XP_005268048.2:p.Asn693Ile
XM_005267992.3:c.2072A>T	XP_005268049.2:p.Asn691Ile
XM_011537067.2:c.2021A>T	XP_011535369.1:p.Asn674Ile
XM_011537069.2:c.2069A>T	XP_011535371.2:p.Asn690Ile
XM_011537070.2:c.1925A>T	XP_011535372.1:p.Asn642Ile
XM_011537071.2:c.1979A>T	XP_011535373.2:p.Asn660Ile
XM_011537072.2:c.1871A>T	XP_011535374.1:p.Asn624Ile
XM_017021582.1:c.2129A>T	XP_016877071.1:p.Asn710Ile
XM_017021583.1:c.2120A>T	XP_016877072.1:p.Asn707Ile
XM_017021584.1:c.2039A>T	XP_016877073.1:p.Asn680Ile
XM_017021585.1:c.1988A>T	XP_016877074.1:p.Asn663Ile
XM_017021586.1:c.1664A>T	XP_016877075.1:p.Asn555Ile
XM_017021587.1:c.1664A>T	XP_016877076.1:p.Asn555Ile
XM_017021588.1:c.1664A>T	XP_016877077.1:p.Asn555Ile
NM_001164749.2:c.1970A>T MANE Select	NP_001158221.1:p.Asn657Ile
NM_001165893.2:c.1880A>T	NP_001159365.1:p.Asn627Ile
NM_022123.3:c.1874A>T	NP_071406.1:p.Asn625Ile
NM_173159.3:c.1931A>T	NP_775182.1:p.Asn644Ile
NM_001394988.1:c.1925A>T	NP_001381917.1:p.Asn642Ile
NM_001394989.1:c.1871A>T	NP_001381918.1:p.Asn624Ile