Canonical Allele Identifier: CA360154869

Gene: POLK

Linked Data

• gnomAD v4: 5-75597771-C-A
• MyVariant Identifiers: chr5:g.74893596C>A (hg19) ; chr5:g.75597771C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.75597771C>A , CM000667.2:g.75597771C>A	GRCh38
NC_000005.9:g.74893596C>A , CM000667.1:g.74893596C>A	GRCh37
NC_000005.8:g.74929352C>A	NCBI36
NG_051590.1:g.91022C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241436.9:c.2510C>A MANE Select	ENSP00000241436.4:p.Ala837Asp
ENST00000241436.8:c.2510C>A	ENSP00000241436.4:p.Ala837Asp
ENST00000502567.1:n.355C>A
ENST00000503479.6:c.*1033C>A	ENSP00000421997.2:n.*1033C>A
ENST00000504026.5:c.1381C>A	ENSP00000425075.1:p.Leu461Met
ENST00000505069.1:n.90C>A
ENST00000505975.5:c.2624C>A	ENSP00000424859.1:n.2624C>A
ENST00000506928.5:n.2633C>A
ENST00000508526.5:c.1916C>A	ENSP00000426853.1:p.Ala639Asp
ENST00000509126.2:c.2338C>A	ENSP00000423532.1:n.2338C>A
ENST00000510815.6:c.*1033C>A	ENSP00000422094.2:n.*1033C>A
ENST00000511527.5:c.1495C>A	ENSP00000420997.1:n.1495C>A
ENST00000514141.5:c.*1129C>A	ENSP00000423526.1:n.*1129C>A
NM_016218.2:c.2510C>A	NP_057302.1:p.Ala837Asp
XM_005248534.3:c.2552C>A	XP_005248591.1:p.Ala851Asp
XM_006714652.2:c.1265C>A	XP_006714715.1:p.Ala422Asp
XM_011543463.1:c.2552C>A	XP_011541765.1:p.Ala851Asp
XM_011543464.1:c.2552C>A	XP_011541766.1:p.Ala851Asp
XM_011543465.1:c.2552C>A	XP_011541767.1:p.Ala851Asp
XM_011543466.1:c.2552C>A	XP_011541768.1:p.Ala851Asp
XM_011543467.1:c.2282C>A	XP_011541769.1:p.Ala761Asp
XR_241784.1:n.2518C>A
XR_948273.1:n.2702C>A
NM_001345921.1:c.2312C>A	NP_001332850.1:p.Ala771Asp
NM_001345922.1:c.2240C>A	NP_001332851.1:p.Ala747Asp
NM_016218.3:c.2510C>A	NP_057302.1:p.Ala837Asp
NR_144315.1:n.2516C>A
XM_005248534.5:c.2552C>A	XP_005248591.1:p.Ala851Asp
XM_006714652.4:c.1265C>A	XP_006714715.1:p.Ala422Asp
XM_011543463.3:c.2552C>A	XP_011541765.1:p.Ala851Asp
XM_011543464.3:c.2552C>A	XP_011541766.1:p.Ala851Asp
XM_011543467.3:c.2282C>A	XP_011541769.1:p.Ala761Asp
XM_017009559.2:c.2510C>A	XP_016865048.1:p.Ala837Asp
XM_017009560.2:c.2510C>A	XP_016865049.1:p.Ala837Asp
XM_017009561.2:c.2354C>A	XP_016865050.1:p.Ala785Asp
XM_017009563.2:c.2240C>A	XP_016865052.1:p.Ala747Asp
XR_001742105.2:n.3000C>A
XR_001742107.2:n.3084C>A
XR_001742108.2:n.2618C>A
XR_241784.3:n.3042C>A
XR_948273.3:n.2702C>A
NM_001345921.2:c.2312C>A	NP_001332850.1:p.Ala771Asp
NM_001345922.2:c.2240C>A	NP_001332851.1:p.Ala747Asp
NM_001387110.2:c.2501C>A	NP_001374039.1:p.Ala834Asp
NM_001387111.2:c.2552C>A	NP_001374040.1:p.Ala851Asp
NM_001387113.2:c.2510C>A	NP_001374042.1:p.Ala837Asp
NM_016218.5:c.2510C>A	NP_057302.1:p.Ala837Asp
NR_144315.2:n.2375C>A
NR_170559.2:n.2364C>A
NR_170560.2:n.2596C>A
NM_001345921.3:c.2312C>A	NP_001332850.1:p.Ala771Asp
NM_001345922.3:c.2240C>A	NP_001332851.1:p.Ala747Asp
NM_001387110.3:c.2501C>A	NP_001374039.1:p.Ala834Asp
NM_001387111.3:c.2552C>A	NP_001374040.1:p.Ala851Asp
NM_001387113.3:c.2510C>A	NP_001374042.1:p.Ala837Asp
NM_001395893.1:c.2240C>A	NP_001382822.1:p.Ala747Asp
NM_001395894.1:c.2552C>A	NP_001382823.1:p.Ala851Asp
NM_001395897.1:c.2549C>A	NP_001382826.1:p.Ala850Asp
NM_001395899.1:c.2357C>A	NP_001382828.1:p.Ala786Asp
NM_001395900.1:c.2312C>A	NP_001382829.1:p.Ala771Asp
NM_001395901.1:c.2270C>A	NP_001382830.1:p.Ala757Asp
NM_001395902.1:c.2240C>A	NP_001382831.1:p.Ala747Asp
NM_016218.6:c.2510C>A MANE Select	NP_057302.1:p.Ala837Asp
NR_144315.3:n.2375C>A
NR_170559.3:n.2364C>A
NR_170560.3:n.2596C>A