Canonical Allele Identifier: CA1556178905
Gene: POLK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.75597985T= , CM000667.2:g.75597985T= GRCh38
NC_000005.9:g.74893810T= , CM000667.1:g.74893810T= GRCh37
NC_000005.8:g.74929566T= NCBI36
NG_051590.1:g.91236T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000241436.9:c.2580T= MANE Select ENSP00000241436.4:p.Asn860=
ENST00000241436.8:c.2580T= ENSP00000241436.4:p.Asn860=
ENST00000502567.1:n.425T=
ENST00000503479.6:c.*1103T= ENSP00000421997.2:n.*1103T=
ENST00000504026.5:c.1451T= ENSP00000425075.1:n.1451T=
ENST00000505069.1:n.304T=
ENST00000505975.5:c.2694T= ENSP00000424859.1:n.2694T=
ENST00000506928.5:n.2703T=
ENST00000508526.5:c.1986T= ENSP00000426853.1:p.Asn662=
ENST00000509126.2:c.2408T= ENSP00000423532.1:n.2408T=
ENST00000510815.6:c.*1103T= ENSP00000422094.2:n.*1103T=
ENST00000511527.5:c.1565T= ENSP00000420997.1:n.1565T=
ENST00000514141.5:c.*1199T= ENSP00000423526.1:n.*1199T=
NM_016218.2:c.2580T= NP_057302.1:p.Asn860=
XM_005248534.3:c.2622T= XP_005248591.1:p.Asn874=
XM_006714652.2:c.1335T= XP_006714715.1:p.Asn445=
XM_011543463.1:c.2622T= XP_011541765.1:p.Asn874=
XM_011543464.1:c.2622T= XP_011541766.1:p.Asn874=
XM_011543465.1:c.2622T= XP_011541767.1:p.Asn874=
XM_011543466.1:c.2622T= XP_011541768.1:p.Asn874=
XM_011543467.1:c.2352T= XP_011541769.1:p.Asn784=
XR_241784.1:n.2588T=
XR_948273.1:n.2772T=
NM_001345921.1:c.2382T= NP_001332850.1:p.Asn794=
NM_001345922.1:c.2310T= NP_001332851.1:p.Asn770=
NM_016218.3:c.2580T= NP_057302.1:p.Asn860=
NR_144315.1:n.2586T=
XM_005248534.5:c.2622T= XP_005248591.1:p.Asn874=
XM_006714652.4:c.1335T= XP_006714715.1:p.Asn445=
XM_011543463.3:c.2622T= XP_011541765.1:p.Asn874=
XM_011543464.3:c.2622T= XP_011541766.1:p.Asn874=
XM_011543467.3:c.2352T= XP_011541769.1:p.Asn784=
XM_017009559.2:c.2580T= XP_016865048.1:p.Asn860=
XM_017009560.2:c.2580T= XP_016865049.1:p.Asn860=
XM_017009561.2:c.2424T= XP_016865050.1:p.Asn808=
XM_017009563.2:c.2310T= XP_016865052.1:p.Asn770=
XR_001742105.2:n.3070T=
XR_001742107.2:n.3154T=
XR_001742108.2:n.2688T=
XR_241784.3:n.3112T=
XR_948273.3:n.2772T=
NM_001345921.2:c.2382T= NP_001332850.1:p.Asn794=
NM_001345922.2:c.2310T= NP_001332851.1:p.Asn770=
NM_001387110.2:c.2571T= NP_001374039.1:p.Asn857=
NM_001387111.2:c.2622T= NP_001374040.1:p.Asn874=
NM_001387113.2:c.2580T= NP_001374042.1:p.Asn860=
NM_016218.5:c.2580T= NP_057302.1:p.Asn860=
NR_144315.2:n.2445T=
NR_170559.2:n.2434T=
NR_170560.2:n.2666T=
NM_001345921.3:c.2382T= NP_001332850.1:p.Asn794=
NM_001345922.3:c.2310T= NP_001332851.1:p.Asn770=
NM_001387110.3:c.2571T= NP_001374039.1:p.Asn857=
NM_001387111.3:c.2622T= NP_001374040.1:p.Asn874=
NM_001387113.3:c.2580T= NP_001374042.1:p.Asn860=
NM_001395893.1:c.2310T= NP_001382822.1:p.Asn770=
NM_001395894.1:c.2622T= NP_001382823.1:p.Asn874=
NM_001395897.1:c.2619T= NP_001382826.1:p.Asn873=
NM_001395899.1:c.2427T= NP_001382828.1:p.Asn809=
NM_001395900.1:c.2382T= NP_001382829.1:p.Asn794=
NM_001395901.1:c.2340T= NP_001382830.1:p.Asn780=
NM_001395902.1:c.2310T= NP_001382831.1:p.Asn770=
NM_016218.6:c.2580T= MANE Select NP_057302.1:p.Asn860=
NR_144315.3:n.2445T=
NR_170559.3:n.2434T=
NR_170560.3:n.2666T=