Canonical Allele Identifier: CA389413349

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269489A>T (hg19) ; chr14:g.33800283A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800283A>T , CM000676.2:g.33800283A>T	GRCh38
NC_000014.8:g.34269489A>T , CM000676.1:g.34269489A>T	GRCh37
NC_000014.7:g.33339240A>T	NCBI36
NG_013036.1:g.866031A>T
NG_013036.2:g.866031A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1976A>T MANE Select	ENSP00000348460.4:p.Asp659Val
ENST00000551634.6:c.1985A>T	ENSP00000448373.2:p.Asp662Val
ENST00000680362.1:c.1876A>T
ENST00000681323.1:c.793+2702A>T
ENST00000346562.6:c.1880A>T	ENSP00000319610.5:p.Asp627Val
ENST00000356141.8:c.1976A>T	ENSP00000348460.4:p.Asp659Val
ENST00000357798.9:c.1937A>T	ENSP00000350446.5:p.Asp646Val
ENST00000548645.5:c.1886A>T	ENSP00000448916.1:p.Asp629Val
ENST00000551492.5:c.1991A>T	ENSP00000450392.1:p.Asp664Val
ENST00000551634.5:c.1898A>T	ENSP00000448373.1:p.Asp633Val
NM_001164749.1:c.1976A>T	NP_001158221.1:p.Asp659Val
NM_001165893.1:c.1886A>T	NP_001159365.1:p.Asp629Val
NM_022123.2:c.1880A>T	NP_071406.1:p.Asp627Val
NM_173159.2:c.1937A>T	NP_775182.1:p.Asp646Val
XM_005267991.2:c.1997A>T	XP_005268048.1:p.Asp666Val
XM_005267992.2:c.1991A>T	XP_005268049.1:p.Asp664Val
XM_005267993.2:c.1937A>T	XP_005268050.1:p.Asp646Val
XM_011537067.1:c.2027A>T	XP_011535369.1:p.Asp676Val
XM_011537068.1:c.2018A>T	XP_011535370.1:p.Asp673Val
XM_011537069.1:c.1988A>T	XP_011535371.1:p.Asp663Val
XM_011537070.1:c.1931A>T	XP_011535372.1:p.Asp644Val
XM_011537071.1:c.1898A>T	XP_011535373.1:p.Asp633Val
XM_011537072.1:c.1877A>T	XP_011535374.1:p.Asp626Val
XM_011537073.1:c.1670A>T	XP_011535375.1:p.Asp557Val
XM_011537074.1:c.1670A>T	XP_011535376.1:p.Asp557Val
XM_005267991.3:c.2084A>T	XP_005268048.2:p.Asp695Val
XM_005267992.3:c.2078A>T	XP_005268049.2:p.Asp693Val
XM_011537067.2:c.2027A>T	XP_011535369.1:p.Asp676Val
XM_011537069.2:c.2075A>T	XP_011535371.2:p.Asp692Val
XM_011537070.2:c.1931A>T	XP_011535372.1:p.Asp644Val
XM_011537071.2:c.1985A>T	XP_011535373.2:p.Asp662Val
XM_011537072.2:c.1877A>T	XP_011535374.1:p.Asp626Val
XM_017021582.1:c.2135A>T	XP_016877071.1:p.Asp712Val
XM_017021583.1:c.2126A>T	XP_016877072.1:p.Asp709Val
XM_017021584.1:c.2045A>T	XP_016877073.1:p.Asp682Val
XM_017021585.1:c.1994A>T	XP_016877074.1:p.Asp665Val
XM_017021586.1:c.1670A>T	XP_016877075.1:p.Asp557Val
XM_017021587.1:c.1670A>T	XP_016877076.1:p.Asp557Val
XM_017021588.1:c.1670A>T	XP_016877077.1:p.Asp557Val
NM_001164749.2:c.1976A>T MANE Select	NP_001158221.1:p.Asp659Val
NM_001165893.2:c.1886A>T	NP_001159365.1:p.Asp629Val
NM_022123.3:c.1880A>T	NP_071406.1:p.Asp627Val
NM_173159.3:c.1937A>T	NP_775182.1:p.Asp646Val
NM_001394988.1:c.1931A>T	NP_001381917.1:p.Asp644Val
NM_001394989.1:c.1877A>T	NP_001381918.1:p.Asp626Val