Canonical Allele Identifier: CA360155063

Gene: POLK

Linked Data

• dbSNP Id: rs769457645
• gnomAD v2: 5-74893821-C-T
• gnomAD v4: 5-75597996-C-T
• MyVariant Identifiers: chr5:g.74893821C>T (hg19) ; chr5:g.75597996C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.75597996C>T , CM000667.2:g.75597996C>T	GRCh38
NC_000005.9:g.74893821C>T , CM000667.1:g.74893821C>T	GRCh37
NC_000005.8:g.74929577C>T	NCBI36
NG_051590.1:g.91247C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000241436.9:c.2591C>T MANE Select	ENSP00000241436.4:p.Thr864Ile
ENST00000241436.8:c.2591C>T	ENSP00000241436.4:p.Thr864Ile
ENST00000503479.6:c.*1114C>T	ENSP00000421997.2:n.*1114C>T
ENST00000504026.5:c.1462C>T	ENSP00000425075.1:n.1462C>T
ENST00000505069.1:n.315C>T
ENST00000505975.5:c.2705C>T	ENSP00000424859.1:n.2705C>T
ENST00000506928.5:n.2714C>T
ENST00000508526.5:c.1997C>T	ENSP00000426853.1:p.Thr666Ile
ENST00000509126.2:c.2419C>T	ENSP00000423532.1:n.2419C>T
ENST00000510815.6:c.*1114C>T	ENSP00000422094.2:n.*1114C>T
ENST00000511527.5:c.1576C>T	ENSP00000420997.1:n.1576C>T
ENST00000514141.5:c.*1210C>T	ENSP00000423526.1:n.*1210C>T
NM_016218.2:c.2591C>T	NP_057302.1:p.Thr864Ile
XM_005248534.3:c.2633C>T	XP_005248591.1:p.Thr878Ile
XM_006714652.2:c.1346C>T	XP_006714715.1:p.Thr449Ile
XM_011543463.1:c.2633C>T	XP_011541765.1:p.Thr878Ile
XM_011543464.1:c.2633C>T	XP_011541766.1:p.Thr878Ile
XM_011543465.1:c.2633C>T	XP_011541767.1:p.Thr878Ile
XM_011543466.1:c.2633C>T	XP_011541768.1:p.Thr878Ile
XM_011543467.1:c.2363C>T	XP_011541769.1:p.Thr788Ile
XR_241784.1:n.2599C>T
XR_948273.1:n.2783C>T
NM_001345921.1:c.2393C>T	NP_001332850.1:p.Thr798Ile
NM_001345922.1:c.2321C>T	NP_001332851.1:p.Thr774Ile
NM_016218.3:c.2591C>T	NP_057302.1:p.Thr864Ile
NR_144315.1:n.2597C>T
XM_005248534.5:c.2633C>T	XP_005248591.1:p.Thr878Ile
XM_006714652.4:c.1346C>T	XP_006714715.1:p.Thr449Ile
XM_011543463.3:c.2633C>T	XP_011541765.1:p.Thr878Ile
XM_011543464.3:c.2633C>T	XP_011541766.1:p.Thr878Ile
XM_011543467.3:c.2363C>T	XP_011541769.1:p.Thr788Ile
XM_017009559.2:c.2591C>T	XP_016865048.1:p.Thr864Ile
XM_017009560.2:c.2591C>T	XP_016865049.1:p.Thr864Ile
XM_017009561.2:c.2435C>T	XP_016865050.1:p.Thr812Ile
XM_017009563.2:c.2321C>T	XP_016865052.1:p.Thr774Ile
XR_001742105.2:n.3081C>T
XR_001742107.2:n.3165C>T
XR_001742108.2:n.2699C>T
XR_241784.3:n.3123C>T
XR_948273.3:n.2783C>T
NM_001345921.2:c.2393C>T	NP_001332850.1:p.Thr798Ile
NM_001345922.2:c.2321C>T	NP_001332851.1:p.Thr774Ile
NM_001387110.2:c.2582C>T	NP_001374039.1:p.Thr861Ile
NM_001387111.2:c.2633C>T	NP_001374040.1:p.Thr878Ile
NM_001387113.2:c.2591C>T	NP_001374042.1:p.Thr864Ile
NM_016218.5:c.2591C>T	NP_057302.1:p.Thr864Ile
NR_144315.2:n.2456C>T
NR_170559.2:n.2445C>T
NR_170560.2:n.2677C>T
NM_001345921.3:c.2393C>T	NP_001332850.1:p.Thr798Ile
NM_001345922.3:c.2321C>T	NP_001332851.1:p.Thr774Ile
NM_001387110.3:c.2582C>T	NP_001374039.1:p.Thr861Ile
NM_001387111.3:c.2633C>T	NP_001374040.1:p.Thr878Ile
NM_001387113.3:c.2591C>T	NP_001374042.1:p.Thr864Ile
NM_001395893.1:c.2321C>T	NP_001382822.1:p.Thr774Ile
NM_001395894.1:c.2633C>T	NP_001382823.1:p.Thr878Ile
NM_001395897.1:c.2630C>T	NP_001382826.1:p.Thr877Ile
NM_001395899.1:c.2438C>T	NP_001382828.1:p.Thr813Ile
NM_001395900.1:c.2393C>T	NP_001382829.1:p.Thr798Ile
NM_001395901.1:c.2351C>T	NP_001382830.1:p.Thr784Ile
NM_001395902.1:c.2321C>T	NP_001382831.1:p.Thr774Ile
NM_016218.6:c.2591C>T MANE Select	NP_057302.1:p.Thr864Ile
NR_144315.3:n.2456C>T
NR_170559.3:n.2445C>T
NR_170560.3:n.2677C>T