Canonical Allele Identifier: CA389413368

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269493T>G (hg19) ; chr14:g.33800287T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800287T>G , CM000676.2:g.33800287T>G	GRCh38
NC_000014.8:g.34269493T>G , CM000676.1:g.34269493T>G	GRCh37
NC_000014.7:g.33339244T>G	NCBI36
NG_013036.1:g.866035T>G
NG_013036.2:g.866035T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1980T>G MANE Select	ENSP00000348460.4:p.Asn660Lys
ENST00000551634.6:c.1989T>G	ENSP00000448373.2:p.Asn663Lys
ENST00000680362.1:c.1880T>G
ENST00000681323.1:c.793+2706T>G
ENST00000346562.6:c.1884T>G	ENSP00000319610.5:p.Asn628Lys
ENST00000356141.8:c.1980T>G	ENSP00000348460.4:p.Asn660Lys
ENST00000357798.9:c.1941T>G	ENSP00000350446.5:p.Asn647Lys
ENST00000548645.5:c.1890T>G	ENSP00000448916.1:p.Asn630Lys
ENST00000551492.5:c.1995T>G	ENSP00000450392.1:p.Asn665Lys
ENST00000551634.5:c.1902T>G	ENSP00000448373.1:p.Asn634Lys
NM_001164749.1:c.1980T>G	NP_001158221.1:p.Asn660Lys
NM_001165893.1:c.1890T>G	NP_001159365.1:p.Asn630Lys
NM_022123.2:c.1884T>G	NP_071406.1:p.Asn628Lys
NM_173159.2:c.1941T>G	NP_775182.1:p.Asn647Lys
XM_005267991.2:c.2001T>G	XP_005268048.1:p.Asn667Lys
XM_005267992.2:c.1995T>G	XP_005268049.1:p.Asn665Lys
XM_005267993.2:c.1941T>G	XP_005268050.1:p.Asn647Lys
XM_011537067.1:c.2031T>G	XP_011535369.1:p.Asn677Lys
XM_011537068.1:c.2022T>G	XP_011535370.1:p.Asn674Lys
XM_011537069.1:c.1992T>G	XP_011535371.1:p.Asn664Lys
XM_011537070.1:c.1935T>G	XP_011535372.1:p.Asn645Lys
XM_011537071.1:c.1902T>G	XP_011535373.1:p.Asn634Lys
XM_011537072.1:c.1881T>G	XP_011535374.1:p.Asn627Lys
XM_011537073.1:c.1674T>G	XP_011535375.1:p.Asn558Lys
XM_011537074.1:c.1674T>G	XP_011535376.1:p.Asn558Lys
XM_005267991.3:c.2088T>G	XP_005268048.2:p.Asn696Lys
XM_005267992.3:c.2082T>G	XP_005268049.2:p.Asn694Lys
XM_011537067.2:c.2031T>G	XP_011535369.1:p.Asn677Lys
XM_011537069.2:c.2079T>G	XP_011535371.2:p.Asn693Lys
XM_011537070.2:c.1935T>G	XP_011535372.1:p.Asn645Lys
XM_011537071.2:c.1989T>G	XP_011535373.2:p.Asn663Lys
XM_011537072.2:c.1881T>G	XP_011535374.1:p.Asn627Lys
XM_017021582.1:c.2139T>G	XP_016877071.1:p.Asn713Lys
XM_017021583.1:c.2130T>G	XP_016877072.1:p.Asn710Lys
XM_017021584.1:c.2049T>G	XP_016877073.1:p.Asn683Lys
XM_017021585.1:c.1998T>G	XP_016877074.1:p.Asn666Lys
XM_017021586.1:c.1674T>G	XP_016877075.1:p.Asn558Lys
XM_017021587.1:c.1674T>G	XP_016877076.1:p.Asn558Lys
XM_017021588.1:c.1674T>G	XP_016877077.1:p.Asn558Lys
NM_001164749.2:c.1980T>G MANE Select	NP_001158221.1:p.Asn660Lys
NM_001165893.2:c.1890T>G	NP_001159365.1:p.Asn630Lys
NM_022123.3:c.1884T>G	NP_071406.1:p.Asn628Lys
NM_173159.3:c.1941T>G	NP_775182.1:p.Asn647Lys
NM_001394988.1:c.1935T>G	NP_001381917.1:p.Asn645Lys
NM_001394989.1:c.1881T>G	NP_001381918.1:p.Asn627Lys