Canonical Allele Identifier: CA3310099

Gene: POLK

Linked Data

• dbSNP Id: rs767783636
• ExAC: 5:74893602 C / T
• gnomAD v2: 5-74893602-C-T
• MyVariant Identifiers: chr5:g.74893602C>T (hg19) ; chr5:g.75597777C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.75597777C>T , CM000667.2:g.75597777C>T	GRCh38
NC_000005.9:g.74893602C>T , CM000667.1:g.74893602C>T	GRCh37
NC_000005.8:g.74929358C>T	NCBI36
NG_051590.1:g.91028C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241436.9:c.2516C>T MANE Select	ENSP00000241436.4:p.Thr839Ile
ENST00000241436.8:c.2516C>T	ENSP00000241436.4:p.Thr839Ile
ENST00000502567.1:n.361C>T
ENST00000503479.6:c.*1039C>T	ENSP00000421997.2:n.*1039C>T
ENST00000504026.5:c.1387C>T	ENSP00000425075.1:n.1387C>T
ENST00000505069.1:n.96C>T
ENST00000505975.5:c.2630C>T	ENSP00000424859.1:n.2630C>T
ENST00000506928.5:n.2639C>T
ENST00000508526.5:c.1922C>T	ENSP00000426853.1:p.Thr641Ile
ENST00000509126.2:c.2344C>T	ENSP00000423532.1:n.2344C>T
ENST00000510815.6:c.*1039C>T	ENSP00000422094.2:n.*1039C>T
ENST00000511527.5:c.1501C>T	ENSP00000420997.1:n.1501C>T
ENST00000514141.5:c.*1135C>T	ENSP00000423526.1:n.*1135C>T
NM_016218.2:c.2516C>T	NP_057302.1:p.Thr839Ile
XM_005248534.3:c.2558C>T	XP_005248591.1:p.Thr853Ile
XM_006714652.2:c.1271C>T	XP_006714715.1:p.Thr424Ile
XM_011543463.1:c.2558C>T	XP_011541765.1:p.Thr853Ile
XM_011543464.1:c.2558C>T	XP_011541766.1:p.Thr853Ile
XM_011543465.1:c.2558C>T	XP_011541767.1:p.Thr853Ile
XM_011543466.1:c.2558C>T	XP_011541768.1:p.Thr853Ile
XM_011543467.1:c.2288C>T	XP_011541769.1:p.Thr763Ile
XR_241784.1:n.2524C>T
XR_948273.1:n.2708C>T
NM_001345921.1:c.2318C>T	NP_001332850.1:p.Thr773Ile
NM_001345922.1:c.2246C>T	NP_001332851.1:p.Thr749Ile
NM_016218.3:c.2516C>T	NP_057302.1:p.Thr839Ile
NR_144315.1:n.2522C>T
XM_005248534.5:c.2558C>T	XP_005248591.1:p.Thr853Ile
XM_006714652.4:c.1271C>T	XP_006714715.1:p.Thr424Ile
XM_011543463.3:c.2558C>T	XP_011541765.1:p.Thr853Ile
XM_011543464.3:c.2558C>T	XP_011541766.1:p.Thr853Ile
XM_011543467.3:c.2288C>T	XP_011541769.1:p.Thr763Ile
XM_017009559.2:c.2516C>T	XP_016865048.1:p.Thr839Ile
XM_017009560.2:c.2516C>T	XP_016865049.1:p.Thr839Ile
XM_017009561.2:c.2360C>T	XP_016865050.1:p.Thr787Ile
XM_017009563.2:c.2246C>T	XP_016865052.1:p.Thr749Ile
XR_001742105.2:n.3006C>T
XR_001742107.2:n.3090C>T
XR_001742108.2:n.2624C>T
XR_241784.3:n.3048C>T
XR_948273.3:n.2708C>T
NM_001345921.2:c.2318C>T	NP_001332850.1:p.Thr773Ile
NM_001345922.2:c.2246C>T	NP_001332851.1:p.Thr749Ile
NM_001387110.2:c.2507C>T	NP_001374039.1:p.Thr836Ile
NM_001387111.2:c.2558C>T	NP_001374040.1:p.Thr853Ile
NM_001387113.2:c.2516C>T	NP_001374042.1:p.Thr839Ile
NM_016218.5:c.2516C>T	NP_057302.1:p.Thr839Ile
NR_144315.2:n.2381C>T
NR_170559.2:n.2370C>T
NR_170560.2:n.2602C>T
NM_001345921.3:c.2318C>T	NP_001332850.1:p.Thr773Ile
NM_001345922.3:c.2246C>T	NP_001332851.1:p.Thr749Ile
NM_001387110.3:c.2507C>T	NP_001374039.1:p.Thr836Ile
NM_001387111.3:c.2558C>T	NP_001374040.1:p.Thr853Ile
NM_001387113.3:c.2516C>T	NP_001374042.1:p.Thr839Ile
NM_001395893.1:c.2246C>T	NP_001382822.1:p.Thr749Ile
NM_001395894.1:c.2558C>T	NP_001382823.1:p.Thr853Ile
NM_001395897.1:c.2555C>T	NP_001382826.1:p.Thr852Ile
NM_001395899.1:c.2363C>T	NP_001382828.1:p.Thr788Ile
NM_001395900.1:c.2318C>T	NP_001382829.1:p.Thr773Ile
NM_001395901.1:c.2276C>T	NP_001382830.1:p.Thr759Ile
NM_001395902.1:c.2246C>T	NP_001382831.1:p.Thr749Ile
NM_016218.6:c.2516C>T MANE Select	NP_057302.1:p.Thr839Ile
NR_144315.3:n.2381C>T
NR_170559.3:n.2370C>T
NR_170560.3:n.2602C>T