Canonical Allele Identifier: CA389413126

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269439T>G (hg19) ; chr14:g.33800233T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800233T>G , CM000676.2:g.33800233T>G	GRCh38
NC_000014.8:g.34269439T>G , CM000676.1:g.34269439T>G	GRCh37
NC_000014.7:g.33339190T>G	NCBI36
NG_013036.1:g.865981T>G
NG_013036.2:g.865981T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1926T>G MANE Select	ENSP00000348460.4:p.Ser642Arg
ENST00000551634.6:c.1935T>G	ENSP00000448373.2:p.Ser645Arg
ENST00000680362.1:c.1826T>G
ENST00000681323.1:c.793+2652T>G
ENST00000346562.6:c.1830T>G	ENSP00000319610.5:p.Ser610Arg
ENST00000356141.8:c.1926T>G	ENSP00000348460.4:p.Ser642Arg
ENST00000357798.9:c.1887T>G	ENSP00000350446.5:p.Ser629Arg
ENST00000548645.5:c.1836T>G	ENSP00000448916.1:p.Ser612Arg
ENST00000551492.5:c.1941T>G	ENSP00000450392.1:p.Ser647Arg
ENST00000551634.5:c.1848T>G	ENSP00000448373.1:p.Ser616Arg
NM_001164749.1:c.1926T>G	NP_001158221.1:p.Ser642Arg
NM_001165893.1:c.1836T>G	NP_001159365.1:p.Ser612Arg
NM_022123.2:c.1830T>G	NP_071406.1:p.Ser610Arg
NM_173159.2:c.1887T>G	NP_775182.1:p.Ser629Arg
XM_005267991.2:c.1947T>G	XP_005268048.1:p.Ser649Arg
XM_005267992.2:c.1941T>G	XP_005268049.1:p.Ser647Arg
XM_005267993.2:c.1887T>G	XP_005268050.1:p.Ser629Arg
XM_011537067.1:c.1977T>G	XP_011535369.1:p.Ser659Arg
XM_011537068.1:c.1968T>G	XP_011535370.1:p.Ser656Arg
XM_011537069.1:c.1938T>G	XP_011535371.1:p.Ser646Arg
XM_011537070.1:c.1881T>G	XP_011535372.1:p.Ser627Arg
XM_011537071.1:c.1848T>G	XP_011535373.1:p.Ser616Arg
XM_011537072.1:c.1827T>G	XP_011535374.1:p.Ser609Arg
XM_011537073.1:c.1620T>G	XP_011535375.1:p.Ser540Arg
XM_011537074.1:c.1620T>G	XP_011535376.1:p.Ser540Arg
XM_005267991.3:c.2034T>G	XP_005268048.2:p.Ser678Arg
XM_005267992.3:c.2028T>G	XP_005268049.2:p.Ser676Arg
XM_011537067.2:c.1977T>G	XP_011535369.1:p.Ser659Arg
XM_011537069.2:c.2025T>G	XP_011535371.2:p.Ser675Arg
XM_011537070.2:c.1881T>G	XP_011535372.1:p.Ser627Arg
XM_011537071.2:c.1935T>G	XP_011535373.2:p.Ser645Arg
XM_011537072.2:c.1827T>G	XP_011535374.1:p.Ser609Arg
XM_017021582.1:c.2085T>G	XP_016877071.1:p.Ser695Arg
XM_017021583.1:c.2076T>G	XP_016877072.1:p.Ser692Arg
XM_017021584.1:c.1995T>G	XP_016877073.1:p.Ser665Arg
XM_017021585.1:c.1944T>G	XP_016877074.1:p.Ser648Arg
XM_017021586.1:c.1620T>G	XP_016877075.1:p.Ser540Arg
XM_017021587.1:c.1620T>G	XP_016877076.1:p.Ser540Arg
XM_017021588.1:c.1620T>G	XP_016877077.1:p.Ser540Arg
NM_001164749.2:c.1926T>G MANE Select	NP_001158221.1:p.Ser642Arg
NM_001165893.2:c.1836T>G	NP_001159365.1:p.Ser612Arg
NM_022123.3:c.1830T>G	NP_071406.1:p.Ser610Arg
NM_173159.3:c.1887T>G	NP_775182.1:p.Ser629Arg
NM_001394988.1:c.1881T>G	NP_001381917.1:p.Ser627Arg
NM_001394989.1:c.1827T>G	NP_001381918.1:p.Ser609Arg