Canonical Allele Identifier: CA360154836

Gene: POLK

Linked Data

• gnomAD v4: 5-75597759-G-T
• MyVariant Identifiers: chr5:g.74893584G>T (hg19) ; chr5:g.75597759G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.75597759G>T , CM000667.2:g.75597759G>T	GRCh38
NC_000005.9:g.74893584G>T , CM000667.1:g.74893584G>T	GRCh37
NC_000005.8:g.74929340G>T	NCBI36
NG_051590.1:g.91010G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241436.9:c.2498G>T MANE Select	ENSP00000241436.4:p.Gly833Val
ENST00000241436.8:c.2498G>T	ENSP00000241436.4:p.Gly833Val
ENST00000502567.1:n.343G>T
ENST00000503479.6:c.*1021G>T	ENSP00000421997.2:n.*1021G>T
ENST00000504026.5:c.1369G>T	ENSP00000425075.1:p.Glu457Ter
ENST00000505069.1:n.78G>T
ENST00000505975.5:c.2612G>T	ENSP00000424859.1:n.2612G>T
ENST00000506928.5:n.2621G>T
ENST00000508526.5:c.1904G>T	ENSP00000426853.1:p.Gly635Val
ENST00000509126.2:c.2326G>T	ENSP00000423532.1:n.2326G>T
ENST00000510815.6:c.*1021G>T	ENSP00000422094.2:n.*1021G>T
ENST00000511527.5:c.1483G>T	ENSP00000420997.1:n.1483G>T
ENST00000514141.5:c.*1117G>T	ENSP00000423526.1:n.*1117G>T
NM_016218.2:c.2498G>T	NP_057302.1:p.Gly833Val
XM_005248534.3:c.2540G>T	XP_005248591.1:p.Gly847Val
XM_006714652.2:c.1253G>T	XP_006714715.1:p.Gly418Val
XM_011543463.1:c.2540G>T	XP_011541765.1:p.Gly847Val
XM_011543464.1:c.2540G>T	XP_011541766.1:p.Gly847Val
XM_011543465.1:c.2540G>T	XP_011541767.1:p.Gly847Val
XM_011543466.1:c.2540G>T	XP_011541768.1:p.Gly847Val
XM_011543467.1:c.2270G>T	XP_011541769.1:p.Gly757Val
XR_241784.1:n.2506G>T
XR_948273.1:n.2690G>T
NM_001345921.1:c.2300G>T	NP_001332850.1:p.Gly767Val
NM_001345922.1:c.2228G>T	NP_001332851.1:p.Gly743Val
NM_016218.3:c.2498G>T	NP_057302.1:p.Gly833Val
NR_144315.1:n.2504G>T
XM_005248534.5:c.2540G>T	XP_005248591.1:p.Gly847Val
XM_006714652.4:c.1253G>T	XP_006714715.1:p.Gly418Val
XM_011543463.3:c.2540G>T	XP_011541765.1:p.Gly847Val
XM_011543464.3:c.2540G>T	XP_011541766.1:p.Gly847Val
XM_011543467.3:c.2270G>T	XP_011541769.1:p.Gly757Val
XM_017009559.2:c.2498G>T	XP_016865048.1:p.Gly833Val
XM_017009560.2:c.2498G>T	XP_016865049.1:p.Gly833Val
XM_017009561.2:c.2342G>T	XP_016865050.1:p.Gly781Val
XM_017009563.2:c.2228G>T	XP_016865052.1:p.Gly743Val
XR_001742105.2:n.2988G>T
XR_001742107.2:n.3072G>T
XR_001742108.2:n.2606G>T
XR_241784.3:n.3030G>T
XR_948273.3:n.2690G>T
NM_001345921.2:c.2300G>T	NP_001332850.1:p.Gly767Val
NM_001345922.2:c.2228G>T	NP_001332851.1:p.Gly743Val
NM_001387110.2:c.2489G>T	NP_001374039.1:p.Gly830Val
NM_001387111.2:c.2540G>T	NP_001374040.1:p.Gly847Val
NM_001387113.2:c.2498G>T	NP_001374042.1:p.Gly833Val
NM_016218.5:c.2498G>T	NP_057302.1:p.Gly833Val
NR_144315.2:n.2363G>T
NR_170559.2:n.2352G>T
NR_170560.2:n.2584G>T
NM_001345921.3:c.2300G>T	NP_001332850.1:p.Gly767Val
NM_001345922.3:c.2228G>T	NP_001332851.1:p.Gly743Val
NM_001387110.3:c.2489G>T	NP_001374039.1:p.Gly830Val
NM_001387111.3:c.2540G>T	NP_001374040.1:p.Gly847Val
NM_001387113.3:c.2498G>T	NP_001374042.1:p.Gly833Val
NM_001395893.1:c.2228G>T	NP_001382822.1:p.Gly743Val
NM_001395894.1:c.2540G>T	NP_001382823.1:p.Gly847Val
NM_001395897.1:c.2537G>T	NP_001382826.1:p.Gly846Val
NM_001395899.1:c.2345G>T	NP_001382828.1:p.Gly782Val
NM_001395900.1:c.2300G>T	NP_001382829.1:p.Gly767Val
NM_001395901.1:c.2258G>T	NP_001382830.1:p.Gly753Val
NM_001395902.1:c.2228G>T	NP_001382831.1:p.Gly743Val
NM_016218.6:c.2498G>T MANE Select	NP_057302.1:p.Gly833Val
NR_144315.3:n.2363G>T
NR_170559.3:n.2352G>T
NR_170560.3:n.2584G>T