Canonical Allele Identifier: CA1556178906
Gene: POLK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.75597992C= , CM000667.2:g.75597992C= GRCh38
NC_000005.9:g.74893817C= , CM000667.1:g.74893817C= GRCh37
NC_000005.8:g.74929573C= NCBI36
NG_051590.1:g.91243C=

Transcript Alleles

HGVS Amino-acid change
ENST00000241436.9:c.2587C= MANE Select ENSP00000241436.4:p.His863=
ENST00000241436.8:c.2587C= ENSP00000241436.4:p.His863=
ENST00000503479.6:c.*1110C= ENSP00000421997.2:n.*1110C=
ENST00000504026.5:c.1458C= ENSP00000425075.1:n.1458C=
ENST00000505069.1:n.311C=
ENST00000505975.5:c.2701C= ENSP00000424859.1:n.2701C=
ENST00000506928.5:n.2710C=
ENST00000508526.5:c.1993C= ENSP00000426853.1:p.His665=
ENST00000509126.2:c.2415C= ENSP00000423532.1:n.2415C=
ENST00000510815.6:c.*1110C= ENSP00000422094.2:n.*1110C=
ENST00000511527.5:c.1572C= ENSP00000420997.1:n.1572C=
ENST00000514141.5:c.*1206C= ENSP00000423526.1:n.*1206C=
NM_016218.2:c.2587C= NP_057302.1:p.His863=
XM_005248534.3:c.2629C= XP_005248591.1:p.His877=
XM_006714652.2:c.1342C= XP_006714715.1:p.His448=
XM_011543463.1:c.2629C= XP_011541765.1:p.His877=
XM_011543464.1:c.2629C= XP_011541766.1:p.His877=
XM_011543465.1:c.2629C= XP_011541767.1:p.His877=
XM_011543466.1:c.2629C= XP_011541768.1:p.His877=
XM_011543467.1:c.2359C= XP_011541769.1:p.His787=
XR_241784.1:n.2595C=
XR_948273.1:n.2779C=
NM_001345921.1:c.2389C= NP_001332850.1:p.His797=
NM_001345922.1:c.2317C= NP_001332851.1:p.His773=
NM_016218.3:c.2587C= NP_057302.1:p.His863=
NR_144315.1:n.2593C=
XM_005248534.5:c.2629C= XP_005248591.1:p.His877=
XM_006714652.4:c.1342C= XP_006714715.1:p.His448=
XM_011543463.3:c.2629C= XP_011541765.1:p.His877=
XM_011543464.3:c.2629C= XP_011541766.1:p.His877=
XM_011543467.3:c.2359C= XP_011541769.1:p.His787=
XM_017009559.2:c.2587C= XP_016865048.1:p.His863=
XM_017009560.2:c.2587C= XP_016865049.1:p.His863=
XM_017009561.2:c.2431C= XP_016865050.1:p.His811=
XM_017009563.2:c.2317C= XP_016865052.1:p.His773=
XR_001742105.2:n.3077C=
XR_001742107.2:n.3161C=
XR_001742108.2:n.2695C=
XR_241784.3:n.3119C=
XR_948273.3:n.2779C=
NM_001345921.2:c.2389C= NP_001332850.1:p.His797=
NM_001345922.2:c.2317C= NP_001332851.1:p.His773=
NM_001387110.2:c.2578C= NP_001374039.1:p.His860=
NM_001387111.2:c.2629C= NP_001374040.1:p.His877=
NM_001387113.2:c.2587C= NP_001374042.1:p.His863=
NM_016218.5:c.2587C= NP_057302.1:p.His863=
NR_144315.2:n.2452C=
NR_170559.2:n.2441C=
NR_170560.2:n.2673C=
NM_001345921.3:c.2389C= NP_001332850.1:p.His797=
NM_001345922.3:c.2317C= NP_001332851.1:p.His773=
NM_001387110.3:c.2578C= NP_001374039.1:p.His860=
NM_001387111.3:c.2629C= NP_001374040.1:p.His877=
NM_001387113.3:c.2587C= NP_001374042.1:p.His863=
NM_001395893.1:c.2317C= NP_001382822.1:p.His773=
NM_001395894.1:c.2629C= NP_001382823.1:p.His877=
NM_001395897.1:c.2626C= NP_001382826.1:p.His876=
NM_001395899.1:c.2434C= NP_001382828.1:p.His812=
NM_001395900.1:c.2389C= NP_001382829.1:p.His797=
NM_001395901.1:c.2347C= NP_001382830.1:p.His783=
NM_001395902.1:c.2317C= NP_001382831.1:p.His773=
NM_016218.6:c.2587C= MANE Select NP_057302.1:p.His863=
NR_144315.3:n.2452C=
NR_170559.3:n.2441C=
NR_170560.3:n.2673C=