Canonical Allele Identifier: CA1556178883
Gene: POLK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.75597935C= , CM000667.2:g.75597935C= GRCh38
NC_000005.9:g.74893760C= , CM000667.1:g.74893760C= GRCh37
NC_000005.8:g.74929516C= NCBI36
NG_051590.1:g.91186C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000241436.9:c.2530C= MANE Select ENSP00000241436.4:p.Pro844=
ENST00000241436.8:c.2530C= ENSP00000241436.4:p.Pro844=
ENST00000502567.1:n.375C=
ENST00000503479.6:c.*1053C= ENSP00000421997.2:n.*1053C=
ENST00000504026.5:c.1401C= ENSP00000425075.1:n.1401C=
ENST00000505069.1:n.254C=
ENST00000505975.5:c.2644C= ENSP00000424859.1:n.2644C=
ENST00000506928.5:n.2653C=
ENST00000508526.5:c.1936C= ENSP00000426853.1:p.Pro646=
ENST00000509126.2:c.2358C= ENSP00000423532.1:n.2358C=
ENST00000510815.6:c.*1053C= ENSP00000422094.2:n.*1053C=
ENST00000511527.5:c.1515C= ENSP00000420997.1:n.1515C=
ENST00000514141.5:c.*1149C= ENSP00000423526.1:n.*1149C=
NM_016218.2:c.2530C= NP_057302.1:p.Pro844=
XM_005248534.3:c.2572C= XP_005248591.1:p.Pro858=
XM_006714652.2:c.1285C= XP_006714715.1:p.Pro429=
XM_011543463.1:c.2572C= XP_011541765.1:p.Pro858=
XM_011543464.1:c.2572C= XP_011541766.1:p.Pro858=
XM_011543465.1:c.2572C= XP_011541767.1:p.Pro858=
XM_011543466.1:c.2572C= XP_011541768.1:p.Pro858=
XM_011543467.1:c.2302C= XP_011541769.1:p.Pro768=
XR_241784.1:n.2538C=
XR_948273.1:n.2722C=
NM_001345921.1:c.2332C= NP_001332850.1:p.Pro778=
NM_001345922.1:c.2260C= NP_001332851.1:p.Pro754=
NM_016218.3:c.2530C= NP_057302.1:p.Pro844=
NR_144315.1:n.2536C=
XM_005248534.5:c.2572C= XP_005248591.1:p.Pro858=
XM_006714652.4:c.1285C= XP_006714715.1:p.Pro429=
XM_011543463.3:c.2572C= XP_011541765.1:p.Pro858=
XM_011543464.3:c.2572C= XP_011541766.1:p.Pro858=
XM_011543467.3:c.2302C= XP_011541769.1:p.Pro768=
XM_017009559.2:c.2530C= XP_016865048.1:p.Pro844=
XM_017009560.2:c.2530C= XP_016865049.1:p.Pro844=
XM_017009561.2:c.2374C= XP_016865050.1:p.Pro792=
XM_017009563.2:c.2260C= XP_016865052.1:p.Pro754=
XR_001742105.2:n.3020C=
XR_001742107.2:n.3104C=
XR_001742108.2:n.2638C=
XR_241784.3:n.3062C=
XR_948273.3:n.2722C=
NM_001345921.2:c.2332C= NP_001332850.1:p.Pro778=
NM_001345922.2:c.2260C= NP_001332851.1:p.Pro754=
NM_001387110.2:c.2521C= NP_001374039.1:p.Pro841=
NM_001387111.2:c.2572C= NP_001374040.1:p.Pro858=
NM_001387113.2:c.2530C= NP_001374042.1:p.Pro844=
NM_016218.5:c.2530C= NP_057302.1:p.Pro844=
NR_144315.2:n.2395C=
NR_170559.2:n.2384C=
NR_170560.2:n.2616C=
NM_001345921.3:c.2332C= NP_001332850.1:p.Pro778=
NM_001345922.3:c.2260C= NP_001332851.1:p.Pro754=
NM_001387110.3:c.2521C= NP_001374039.1:p.Pro841=
NM_001387111.3:c.2572C= NP_001374040.1:p.Pro858=
NM_001387113.3:c.2530C= NP_001374042.1:p.Pro844=
NM_001395893.1:c.2260C= NP_001382822.1:p.Pro754=
NM_001395894.1:c.2572C= NP_001382823.1:p.Pro858=
NM_001395897.1:c.2569C= NP_001382826.1:p.Pro857=
NM_001395899.1:c.2377C= NP_001382828.1:p.Pro793=
NM_001395900.1:c.2332C= NP_001382829.1:p.Pro778=
NM_001395901.1:c.2290C= NP_001382830.1:p.Pro764=
NM_001395902.1:c.2260C= NP_001382831.1:p.Pro754=
NM_016218.6:c.2530C= MANE Select NP_057302.1:p.Pro844=
NR_144315.3:n.2395C=
NR_170559.3:n.2384C=
NR_170560.3:n.2616C=