Canonical Allele Identifier: CA1556178828
Gene: POLK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.75597783C= , CM000667.2:g.75597783C= GRCh38
NC_000005.9:g.74893608C= , CM000667.1:g.74893608C= GRCh37
NC_000005.8:g.74929364C= NCBI36
NG_051590.1:g.91034C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000241436.9:c.2522C= MANE Select ENSP00000241436.4:p.Thr841=
ENST00000241436.8:c.2522C= ENSP00000241436.4:p.Thr841=
ENST00000502567.1:n.367C=
ENST00000503479.6:c.*1045C= ENSP00000421997.2:n.*1045C=
ENST00000504026.5:c.1393C= ENSP00000425075.1:n.1393C=
ENST00000505069.1:n.102C=
ENST00000505975.5:c.2636C= ENSP00000424859.1:n.2636C=
ENST00000506928.5:n.2645C=
ENST00000508526.5:c.1928C= ENSP00000426853.1:p.Thr643=
ENST00000509126.2:c.2350C= ENSP00000423532.1:n.2350C=
ENST00000510815.6:c.*1045C= ENSP00000422094.2:n.*1045C=
ENST00000511527.5:c.1507C= ENSP00000420997.1:n.1507C=
ENST00000514141.5:c.*1141C= ENSP00000423526.1:n.*1141C=
NM_016218.2:c.2522C= NP_057302.1:p.Thr841=
XM_005248534.3:c.2564C= XP_005248591.1:p.Thr855=
XM_006714652.2:c.1277C= XP_006714715.1:p.Thr426=
XM_011543463.1:c.2564C= XP_011541765.1:p.Thr855=
XM_011543464.1:c.2564C= XP_011541766.1:p.Thr855=
XM_011543465.1:c.2564C= XP_011541767.1:p.Thr855=
XM_011543466.1:c.2564C= XP_011541768.1:p.Thr855=
XM_011543467.1:c.2294C= XP_011541769.1:p.Thr765=
XR_241784.1:n.2530C=
XR_948273.1:n.2714C=
NM_001345921.1:c.2324C= NP_001332850.1:p.Thr775=
NM_001345922.1:c.2252C= NP_001332851.1:p.Thr751=
NM_016218.3:c.2522C= NP_057302.1:p.Thr841=
NR_144315.1:n.2528C=
XM_005248534.5:c.2564C= XP_005248591.1:p.Thr855=
XM_006714652.4:c.1277C= XP_006714715.1:p.Thr426=
XM_011543463.3:c.2564C= XP_011541765.1:p.Thr855=
XM_011543464.3:c.2564C= XP_011541766.1:p.Thr855=
XM_011543467.3:c.2294C= XP_011541769.1:p.Thr765=
XM_017009559.2:c.2522C= XP_016865048.1:p.Thr841=
XM_017009560.2:c.2522C= XP_016865049.1:p.Thr841=
XM_017009561.2:c.2366C= XP_016865050.1:p.Thr789=
XM_017009563.2:c.2252C= XP_016865052.1:p.Thr751=
XR_001742105.2:n.3012C=
XR_001742107.2:n.3096C=
XR_001742108.2:n.2630C=
XR_241784.3:n.3054C=
XR_948273.3:n.2714C=
NM_001345921.2:c.2324C= NP_001332850.1:p.Thr775=
NM_001345922.2:c.2252C= NP_001332851.1:p.Thr751=
NM_001387110.2:c.2513C= NP_001374039.1:p.Thr838=
NM_001387111.2:c.2564C= NP_001374040.1:p.Thr855=
NM_001387113.2:c.2522C= NP_001374042.1:p.Thr841=
NM_016218.5:c.2522C= NP_057302.1:p.Thr841=
NR_144315.2:n.2387C=
NR_170559.2:n.2376C=
NR_170560.2:n.2608C=
NM_001345921.3:c.2324C= NP_001332850.1:p.Thr775=
NM_001345922.3:c.2252C= NP_001332851.1:p.Thr751=
NM_001387110.3:c.2513C= NP_001374039.1:p.Thr838=
NM_001387111.3:c.2564C= NP_001374040.1:p.Thr855=
NM_001387113.3:c.2522C= NP_001374042.1:p.Thr841=
NM_001395893.1:c.2252C= NP_001382822.1:p.Thr751=
NM_001395894.1:c.2564C= NP_001382823.1:p.Thr855=
NM_001395897.1:c.2561C= NP_001382826.1:p.Thr854=
NM_001395899.1:c.2369C= NP_001382828.1:p.Thr790=
NM_001395900.1:c.2324C= NP_001382829.1:p.Thr775=
NM_001395901.1:c.2282C= NP_001382830.1:p.Thr761=
NM_001395902.1:c.2252C= NP_001382831.1:p.Thr751=
NM_016218.6:c.2522C= MANE Select NP_057302.1:p.Thr841=
NR_144315.3:n.2387C=
NR_170559.3:n.2376C=
NR_170560.3:n.2608C=