Canonical Allele Identifier: CA1556178822
Gene: POLK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.75597764C= , CM000667.2:g.75597764C= GRCh38
NC_000005.9:g.74893589C= , CM000667.1:g.74893589C= GRCh37
NC_000005.8:g.74929345C= NCBI36
NG_051590.1:g.91015C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000241436.9:c.2503C= MANE Select ENSP00000241436.4:p.Gln835=
ENST00000241436.8:c.2503C= ENSP00000241436.4:p.Gln835=
ENST00000502567.1:n.348C=
ENST00000503479.6:c.*1026C= ENSP00000421997.2:n.*1026C=
ENST00000504026.5:c.1374C= ENSP00000425075.1:p.Tyr458=
ENST00000505069.1:n.83C=
ENST00000505975.5:c.2617C= ENSP00000424859.1:n.2617C=
ENST00000506928.5:n.2626C=
ENST00000508526.5:c.1909C= ENSP00000426853.1:p.Gln637=
ENST00000509126.2:c.2331C= ENSP00000423532.1:n.2331C=
ENST00000510815.6:c.*1026C= ENSP00000422094.2:n.*1026C=
ENST00000511527.5:c.1488C= ENSP00000420997.1:n.1488C=
ENST00000514141.5:c.*1122C= ENSP00000423526.1:n.*1122C=
NM_016218.2:c.2503C= NP_057302.1:p.Gln835=
XM_005248534.3:c.2545C= XP_005248591.1:p.Gln849=
XM_006714652.2:c.1258C= XP_006714715.1:p.Gln420=
XM_011543463.1:c.2545C= XP_011541765.1:p.Gln849=
XM_011543464.1:c.2545C= XP_011541766.1:p.Gln849=
XM_011543465.1:c.2545C= XP_011541767.1:p.Gln849=
XM_011543466.1:c.2545C= XP_011541768.1:p.Gln849=
XM_011543467.1:c.2275C= XP_011541769.1:p.Gln759=
XR_241784.1:n.2511C=
XR_948273.1:n.2695C=
NM_001345921.1:c.2305C= NP_001332850.1:p.Gln769=
NM_001345922.1:c.2233C= NP_001332851.1:p.Gln745=
NM_016218.3:c.2503C= NP_057302.1:p.Gln835=
NR_144315.1:n.2509C=
XM_005248534.5:c.2545C= XP_005248591.1:p.Gln849=
XM_006714652.4:c.1258C= XP_006714715.1:p.Gln420=
XM_011543463.3:c.2545C= XP_011541765.1:p.Gln849=
XM_011543464.3:c.2545C= XP_011541766.1:p.Gln849=
XM_011543467.3:c.2275C= XP_011541769.1:p.Gln759=
XM_017009559.2:c.2503C= XP_016865048.1:p.Gln835=
XM_017009560.2:c.2503C= XP_016865049.1:p.Gln835=
XM_017009561.2:c.2347C= XP_016865050.1:p.Gln783=
XM_017009563.2:c.2233C= XP_016865052.1:p.Gln745=
XR_001742105.2:n.2993C=
XR_001742107.2:n.3077C=
XR_001742108.2:n.2611C=
XR_241784.3:n.3035C=
XR_948273.3:n.2695C=
NM_001345921.2:c.2305C= NP_001332850.1:p.Gln769=
NM_001345922.2:c.2233C= NP_001332851.1:p.Gln745=
NM_001387110.2:c.2494C= NP_001374039.1:p.Gln832=
NM_001387111.2:c.2545C= NP_001374040.1:p.Gln849=
NM_001387113.2:c.2503C= NP_001374042.1:p.Gln835=
NM_016218.5:c.2503C= NP_057302.1:p.Gln835=
NR_144315.2:n.2368C=
NR_170559.2:n.2357C=
NR_170560.2:n.2589C=
NM_001345921.3:c.2305C= NP_001332850.1:p.Gln769=
NM_001345922.3:c.2233C= NP_001332851.1:p.Gln745=
NM_001387110.3:c.2494C= NP_001374039.1:p.Gln832=
NM_001387111.3:c.2545C= NP_001374040.1:p.Gln849=
NM_001387113.3:c.2503C= NP_001374042.1:p.Gln835=
NM_001395893.1:c.2233C= NP_001382822.1:p.Gln745=
NM_001395894.1:c.2545C= NP_001382823.1:p.Gln849=
NM_001395897.1:c.2542C= NP_001382826.1:p.Gln848=
NM_001395899.1:c.2350C= NP_001382828.1:p.Gln784=
NM_001395900.1:c.2305C= NP_001382829.1:p.Gln769=
NM_001395901.1:c.2263C= NP_001382830.1:p.Gln755=
NM_001395902.1:c.2233C= NP_001382831.1:p.Gln745=
NM_016218.6:c.2503C= MANE Select NP_057302.1:p.Gln835=
NR_144315.3:n.2368C=
NR_170559.3:n.2357C=
NR_170560.3:n.2589C=