Canonical Allele Identifier: CA389414316
Gene: NPAS3 HGNC NCBI

Linked Data

dbSNP Id: rs1419818068

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.33800571C>T , CM000676.2:g.33800571C>T GRCh38
NC_000014.8:g.34269777C>T , CM000676.1:g.34269777C>T GRCh37
NC_000014.7:g.33339528C>T NCBI36
NG_013036.1:g.866319C>T
NG_013036.2:g.866319C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356141.9:c.2264C>T MANE Select ENSP00000348460.4:p.Pro755Leu
ENST00000551634.6:c.2273C>T ENSP00000448373.2:p.Pro758Leu
ENST00000680362.1:c.2164C>T
ENST00000681323.1:c.793+2990C>T
ENST00000346562.6:c.2168C>T ENSP00000319610.5:p.Pro723Leu
ENST00000356141.8:c.2264C>T ENSP00000348460.4:p.Pro755Leu
ENST00000357798.9:c.2225C>T ENSP00000350446.5:p.Pro742Leu
ENST00000548645.5:c.2174C>T ENSP00000448916.1:p.Pro725Leu
ENST00000551492.5:c.2279C>T ENSP00000450392.1:p.Pro760Leu
ENST00000551634.5:c.2186C>T ENSP00000448373.1:p.Pro729Leu
NM_001164749.1:c.2264C>T NP_001158221.1:p.Pro755Leu
NM_001165893.1:c.2174C>T NP_001159365.1:p.Pro725Leu
NM_022123.2:c.2168C>T NP_071406.1:p.Pro723Leu
NM_173159.2:c.2225C>T NP_775182.1:p.Pro742Leu
XM_005267991.2:c.2285C>T XP_005268048.1:p.Pro762Leu
XM_005267992.2:c.2279C>T XP_005268049.1:p.Pro760Leu
XM_005267993.2:c.2225C>T XP_005268050.1:p.Pro742Leu
XM_011537067.1:c.2315C>T XP_011535369.1:p.Pro772Leu
XM_011537068.1:c.2306C>T XP_011535370.1:p.Pro769Leu
XM_011537069.1:c.2276C>T XP_011535371.1:p.Pro759Leu
XM_011537070.1:c.2219C>T XP_011535372.1:p.Pro740Leu
XM_011537071.1:c.2186C>T XP_011535373.1:p.Pro729Leu
XM_011537072.1:c.2165C>T XP_011535374.1:p.Pro722Leu
XM_011537073.1:c.1958C>T XP_011535375.1:p.Pro653Leu
XM_011537074.1:c.1958C>T XP_011535376.1:p.Pro653Leu
XM_005267991.3:c.2372C>T XP_005268048.2:p.Pro791Leu
XM_005267992.3:c.2366C>T XP_005268049.2:p.Pro789Leu
XM_011537067.2:c.2315C>T XP_011535369.1:p.Pro772Leu
XM_011537069.2:c.2363C>T XP_011535371.2:p.Pro788Leu
XM_011537070.2:c.2219C>T XP_011535372.1:p.Pro740Leu
XM_011537071.2:c.2273C>T XP_011535373.2:p.Pro758Leu
XM_011537072.2:c.2165C>T XP_011535374.1:p.Pro722Leu
XM_017021582.1:c.2423C>T XP_016877071.1:p.Pro808Leu
XM_017021583.1:c.2414C>T XP_016877072.1:p.Pro805Leu
XM_017021584.1:c.2333C>T XP_016877073.1:p.Pro778Leu
XM_017021585.1:c.2282C>T XP_016877074.1:p.Pro761Leu
XM_017021586.1:c.1958C>T XP_016877075.1:p.Pro653Leu
XM_017021587.1:c.1958C>T XP_016877076.1:p.Pro653Leu
XM_017021588.1:c.1958C>T XP_016877077.1:p.Pro653Leu
NM_001164749.2:c.2264C>T MANE Select NP_001158221.1:p.Pro755Leu
NM_001165893.2:c.2174C>T NP_001159365.1:p.Pro725Leu
NM_022123.3:c.2168C>T NP_071406.1:p.Pro723Leu
NM_173159.3:c.2225C>T NP_775182.1:p.Pro742Leu
NM_001394988.1:c.2219C>T NP_001381917.1:p.Pro740Leu
NM_001394989.1:c.2165C>T NP_001381918.1:p.Pro722Leu