Canonical Allele Identifier: CA360154901

Gene: POLK

Linked Data

• MyVariant Identifiers: chr5:g.74893611A>C (hg19) ; chr5:g.75597786A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.75597786A>C , CM000667.2:g.75597786A>C	GRCh38
NC_000005.9:g.74893611A>C , CM000667.1:g.74893611A>C	GRCh37
NC_000005.8:g.74929367A>C	NCBI36
NG_051590.1:g.91037A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241436.9:c.2525A>C MANE Select	ENSP00000241436.4:p.Lys842Thr
ENST00000241436.8:c.2525A>C	ENSP00000241436.4:p.Lys842Thr
ENST00000502567.1:n.370A>C
ENST00000503479.6:c.*1048A>C	ENSP00000421997.2:n.*1048A>C
ENST00000504026.5:c.1396A>C	ENSP00000425075.1:n.1396A>C
ENST00000505069.1:n.105A>C
ENST00000505975.5:c.2639A>C	ENSP00000424859.1:n.2639A>C
ENST00000506928.5:n.2648A>C
ENST00000508526.5:c.1931A>C	ENSP00000426853.1:p.Lys644Thr
ENST00000509126.2:c.2353A>C	ENSP00000423532.1:n.2353A>C
ENST00000510815.6:c.*1048A>C	ENSP00000422094.2:n.*1048A>C
ENST00000511527.5:c.1510A>C	ENSP00000420997.1:n.1510A>C
ENST00000514141.5:c.*1144A>C	ENSP00000423526.1:n.*1144A>C
NM_016218.2:c.2525A>C	NP_057302.1:p.Lys842Thr
XM_005248534.3:c.2567A>C	XP_005248591.1:p.Lys856Thr
XM_006714652.2:c.1280A>C	XP_006714715.1:p.Lys427Thr
XM_011543463.1:c.2567A>C	XP_011541765.1:p.Lys856Thr
XM_011543464.1:c.2567A>C	XP_011541766.1:p.Lys856Thr
XM_011543465.1:c.2567A>C	XP_011541767.1:p.Lys856Thr
XM_011543466.1:c.2567A>C	XP_011541768.1:p.Lys856Thr
XM_011543467.1:c.2297A>C	XP_011541769.1:p.Lys766Thr
XR_241784.1:n.2533A>C
XR_948273.1:n.2717A>C
NM_001345921.1:c.2327A>C	NP_001332850.1:p.Lys776Thr
NM_001345922.1:c.2255A>C	NP_001332851.1:p.Lys752Thr
NM_016218.3:c.2525A>C	NP_057302.1:p.Lys842Thr
NR_144315.1:n.2531A>C
XM_005248534.5:c.2567A>C	XP_005248591.1:p.Lys856Thr
XM_006714652.4:c.1280A>C	XP_006714715.1:p.Lys427Thr
XM_011543463.3:c.2567A>C	XP_011541765.1:p.Lys856Thr
XM_011543464.3:c.2567A>C	XP_011541766.1:p.Lys856Thr
XM_011543467.3:c.2297A>C	XP_011541769.1:p.Lys766Thr
XM_017009559.2:c.2525A>C	XP_016865048.1:p.Lys842Thr
XM_017009560.2:c.2525A>C	XP_016865049.1:p.Lys842Thr
XM_017009561.2:c.2369A>C	XP_016865050.1:p.Lys790Thr
XM_017009563.2:c.2255A>C	XP_016865052.1:p.Lys752Thr
XR_001742105.2:n.3015A>C
XR_001742107.2:n.3099A>C
XR_001742108.2:n.2633A>C
XR_241784.3:n.3057A>C
XR_948273.3:n.2717A>C
NM_001345921.2:c.2327A>C	NP_001332850.1:p.Lys776Thr
NM_001345922.2:c.2255A>C	NP_001332851.1:p.Lys752Thr
NM_001387110.2:c.2516A>C	NP_001374039.1:p.Lys839Thr
NM_001387111.2:c.2567A>C	NP_001374040.1:p.Lys856Thr
NM_001387113.2:c.2525A>C	NP_001374042.1:p.Lys842Thr
NM_016218.5:c.2525A>C	NP_057302.1:p.Lys842Thr
NR_144315.2:n.2390A>C
NR_170559.2:n.2379A>C
NR_170560.2:n.2611A>C
NM_001345921.3:c.2327A>C	NP_001332850.1:p.Lys776Thr
NM_001345922.3:c.2255A>C	NP_001332851.1:p.Lys752Thr
NM_001387110.3:c.2516A>C	NP_001374039.1:p.Lys839Thr
NM_001387111.3:c.2567A>C	NP_001374040.1:p.Lys856Thr
NM_001387113.3:c.2525A>C	NP_001374042.1:p.Lys842Thr
NM_001395893.1:c.2255A>C	NP_001382822.1:p.Lys752Thr
NM_001395894.1:c.2567A>C	NP_001382823.1:p.Lys856Thr
NM_001395897.1:c.2564A>C	NP_001382826.1:p.Lys855Thr
NM_001395899.1:c.2372A>C	NP_001382828.1:p.Lys791Thr
NM_001395900.1:c.2327A>C	NP_001382829.1:p.Lys776Thr
NM_001395901.1:c.2285A>C	NP_001382830.1:p.Lys762Thr
NM_001395902.1:c.2255A>C	NP_001382831.1:p.Lys752Thr
NM_016218.6:c.2525A>C MANE Select	NP_057302.1:p.Lys842Thr
NR_144315.3:n.2390A>C
NR_170559.3:n.2379A>C
NR_170560.3:n.2611A>C