Canonical Allele Identifier: CA360154909

Gene: POLK

Linked Data

• MyVariant Identifiers: chr5:g.74893614G>C (hg19) ; chr5:g.75597789G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.75597789G>C , CM000667.2:g.75597789G>C	GRCh38
NC_000005.9:g.74893614G>C , CM000667.1:g.74893614G>C	GRCh37
NC_000005.8:g.74929370G>C	NCBI36
NG_051590.1:g.91040G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241436.9:c.2528G>C MANE Select	ENSP00000241436.4:p.Arg843Thr
ENST00000241436.8:c.2528G>C	ENSP00000241436.4:p.Arg843Thr
ENST00000502567.1:n.373G>C
ENST00000503479.6:c.*1051G>C	ENSP00000421997.2:n.*1051G>C
ENST00000504026.5:c.1399G>C	ENSP00000425075.1:n.1399G>C
ENST00000505069.1:n.108G>C
ENST00000505975.5:c.2642G>C	ENSP00000424859.1:n.2642G>C
ENST00000506928.5:n.2651G>C
ENST00000508526.5:c.1934G>C	ENSP00000426853.1:p.Arg645Thr
ENST00000509126.2:c.2356G>C	ENSP00000423532.1:n.2356G>C
ENST00000510815.6:c.*1051G>C	ENSP00000422094.2:n.*1051G>C
ENST00000511527.5:c.1513G>C	ENSP00000420997.1:n.1513G>C
ENST00000514141.5:c.*1147G>C	ENSP00000423526.1:n.*1147G>C
NM_016218.2:c.2528G>C	NP_057302.1:p.Arg843Thr
XM_005248534.3:c.2570G>C	XP_005248591.1:p.Arg857Thr
XM_006714652.2:c.1283G>C	XP_006714715.1:p.Arg428Thr
XM_011543463.1:c.2570G>C	XP_011541765.1:p.Arg857Thr
XM_011543464.1:c.2570G>C	XP_011541766.1:p.Arg857Thr
XM_011543465.1:c.2570G>C	XP_011541767.1:p.Arg857Thr
XM_011543466.1:c.2570G>C	XP_011541768.1:p.Arg857Thr
XM_011543467.1:c.2300G>C	XP_011541769.1:p.Arg767Thr
XR_241784.1:n.2536G>C
XR_948273.1:n.2720G>C
NM_001345921.1:c.2330G>C	NP_001332850.1:p.Arg777Thr
NM_001345922.1:c.2258G>C	NP_001332851.1:p.Arg753Thr
NM_016218.3:c.2528G>C	NP_057302.1:p.Arg843Thr
NR_144315.1:n.2534G>C
XM_005248534.5:c.2570G>C	XP_005248591.1:p.Arg857Thr
XM_006714652.4:c.1283G>C	XP_006714715.1:p.Arg428Thr
XM_011543463.3:c.2570G>C	XP_011541765.1:p.Arg857Thr
XM_011543464.3:c.2570G>C	XP_011541766.1:p.Arg857Thr
XM_011543467.3:c.2300G>C	XP_011541769.1:p.Arg767Thr
XM_017009559.2:c.2528G>C	XP_016865048.1:p.Arg843Thr
XM_017009560.2:c.2528G>C	XP_016865049.1:p.Arg843Thr
XM_017009561.2:c.2372G>C	XP_016865050.1:p.Arg791Thr
XM_017009563.2:c.2258G>C	XP_016865052.1:p.Arg753Thr
XR_001742105.2:n.3018G>C
XR_001742107.2:n.3102G>C
XR_001742108.2:n.2636G>C
XR_241784.3:n.3060G>C
XR_948273.3:n.2720G>C
NM_001345921.2:c.2330G>C	NP_001332850.1:p.Arg777Thr
NM_001345922.2:c.2258G>C	NP_001332851.1:p.Arg753Thr
NM_001387110.2:c.2519G>C	NP_001374039.1:p.Arg840Thr
NM_001387111.2:c.2570G>C	NP_001374040.1:p.Arg857Thr
NM_001387113.2:c.2528G>C	NP_001374042.1:p.Arg843Thr
NM_016218.5:c.2528G>C	NP_057302.1:p.Arg843Thr
NR_144315.2:n.2393G>C
NR_170559.2:n.2382G>C
NR_170560.2:n.2614G>C
NM_001345921.3:c.2330G>C	NP_001332850.1:p.Arg777Thr
NM_001345922.3:c.2258G>C	NP_001332851.1:p.Arg753Thr
NM_001387110.3:c.2519G>C	NP_001374039.1:p.Arg840Thr
NM_001387111.3:c.2570G>C	NP_001374040.1:p.Arg857Thr
NM_001387113.3:c.2528G>C	NP_001374042.1:p.Arg843Thr
NM_001395893.1:c.2258G>C	NP_001382822.1:p.Arg753Thr
NM_001395894.1:c.2570G>C	NP_001382823.1:p.Arg857Thr
NM_001395897.1:c.2567G>C	NP_001382826.1:p.Arg856Thr
NM_001395899.1:c.2375G>C	NP_001382828.1:p.Arg792Thr
NM_001395900.1:c.2330G>C	NP_001382829.1:p.Arg777Thr
NM_001395901.1:c.2288G>C	NP_001382830.1:p.Arg763Thr
NM_001395902.1:c.2258G>C	NP_001382831.1:p.Arg753Thr
NM_016218.6:c.2528G>C MANE Select	NP_057302.1:p.Arg843Thr
NR_144315.3:n.2393G>C
NR_170559.3:n.2382G>C
NR_170560.3:n.2614G>C