Canonical Allele Identifier: CA1556178907
Gene: POLK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.75597993A= , CM000667.2:g.75597993A= GRCh38
NC_000005.9:g.74893818A= , CM000667.1:g.74893818A= GRCh37
NC_000005.8:g.74929574A= NCBI36
NG_051590.1:g.91244A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000241436.9:c.2588A= MANE Select ENSP00000241436.4:p.His863=
ENST00000241436.8:c.2588A= ENSP00000241436.4:p.His863=
ENST00000503479.6:c.*1111A= ENSP00000421997.2:n.*1111A=
ENST00000504026.5:c.1459A= ENSP00000425075.1:n.1459A=
ENST00000505069.1:n.312A=
ENST00000505975.5:c.2702A= ENSP00000424859.1:n.2702A=
ENST00000506928.5:n.2711A=
ENST00000508526.5:c.1994A= ENSP00000426853.1:p.His665=
ENST00000509126.2:c.2416A= ENSP00000423532.1:n.2416A=
ENST00000510815.6:c.*1111A= ENSP00000422094.2:n.*1111A=
ENST00000511527.5:c.1573A= ENSP00000420997.1:n.1573A=
ENST00000514141.5:c.*1207A= ENSP00000423526.1:n.*1207A=
NM_016218.2:c.2588A= NP_057302.1:p.His863=
XM_005248534.3:c.2630A= XP_005248591.1:p.His877=
XM_006714652.2:c.1343A= XP_006714715.1:p.His448=
XM_011543463.1:c.2630A= XP_011541765.1:p.His877=
XM_011543464.1:c.2630A= XP_011541766.1:p.His877=
XM_011543465.1:c.2630A= XP_011541767.1:p.His877=
XM_011543466.1:c.2630A= XP_011541768.1:p.His877=
XM_011543467.1:c.2360A= XP_011541769.1:p.His787=
XR_241784.1:n.2596A=
XR_948273.1:n.2780A=
NM_001345921.1:c.2390A= NP_001332850.1:p.His797=
NM_001345922.1:c.2318A= NP_001332851.1:p.His773=
NM_016218.3:c.2588A= NP_057302.1:p.His863=
NR_144315.1:n.2594A=
XM_005248534.5:c.2630A= XP_005248591.1:p.His877=
XM_006714652.4:c.1343A= XP_006714715.1:p.His448=
XM_011543463.3:c.2630A= XP_011541765.1:p.His877=
XM_011543464.3:c.2630A= XP_011541766.1:p.His877=
XM_011543467.3:c.2360A= XP_011541769.1:p.His787=
XM_017009559.2:c.2588A= XP_016865048.1:p.His863=
XM_017009560.2:c.2588A= XP_016865049.1:p.His863=
XM_017009561.2:c.2432A= XP_016865050.1:p.His811=
XM_017009563.2:c.2318A= XP_016865052.1:p.His773=
XR_001742105.2:n.3078A=
XR_001742107.2:n.3162A=
XR_001742108.2:n.2696A=
XR_241784.3:n.3120A=
XR_948273.3:n.2780A=
NM_001345921.2:c.2390A= NP_001332850.1:p.His797=
NM_001345922.2:c.2318A= NP_001332851.1:p.His773=
NM_001387110.2:c.2579A= NP_001374039.1:p.His860=
NM_001387111.2:c.2630A= NP_001374040.1:p.His877=
NM_001387113.2:c.2588A= NP_001374042.1:p.His863=
NM_016218.5:c.2588A= NP_057302.1:p.His863=
NR_144315.2:n.2453A=
NR_170559.2:n.2442A=
NR_170560.2:n.2674A=
NM_001345921.3:c.2390A= NP_001332850.1:p.His797=
NM_001345922.3:c.2318A= NP_001332851.1:p.His773=
NM_001387110.3:c.2579A= NP_001374039.1:p.His860=
NM_001387111.3:c.2630A= NP_001374040.1:p.His877=
NM_001387113.3:c.2588A= NP_001374042.1:p.His863=
NM_001395893.1:c.2318A= NP_001382822.1:p.His773=
NM_001395894.1:c.2630A= NP_001382823.1:p.His877=
NM_001395897.1:c.2627A= NP_001382826.1:p.His876=
NM_001395899.1:c.2435A= NP_001382828.1:p.His812=
NM_001395900.1:c.2390A= NP_001382829.1:p.His797=
NM_001395901.1:c.2348A= NP_001382830.1:p.His783=
NM_001395902.1:c.2318A= NP_001382831.1:p.His773=
NM_016218.6:c.2588A= MANE Select NP_057302.1:p.His863=
NR_144315.3:n.2453A=
NR_170559.3:n.2442A=
NR_170560.3:n.2674A=