Canonical Allele Identifier: CA444695587

Gene: POLK

Linked Data

• gnomAD v4: 5-75597967-G-A
• MyVariant Identifiers: chr5:g.74893792G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.75597967G>A , CM000667.2:g.75597967G>A	GRCh38
NC_000005.9:g.74893792G>A , CM000667.1:g.74893792G>A	GRCh37
NC_000005.8:g.74929548G>A	NCBI36
NG_051590.1:g.91218G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241436.9:c.2562G>A MANE Select	ENSP00000241436.4:p.Lys854=
ENST00000241436.8:c.2562G>A	ENSP00000241436.4:p.Lys854=
ENST00000502567.1:n.407G>A
ENST00000503479.6:c.*1085G>A	ENSP00000421997.2:n.*1085G>A
ENST00000504026.5:c.1433G>A	ENSP00000425075.1:n.1433G>A
ENST00000505069.1:n.286G>A
ENST00000505975.5:c.2676G>A	ENSP00000424859.1:n.2676G>A
ENST00000506928.5:n.2685G>A
ENST00000508526.5:c.1968G>A	ENSP00000426853.1:p.Lys656=
ENST00000509126.2:c.2390G>A	ENSP00000423532.1:n.2390G>A
ENST00000510815.6:c.*1085G>A	ENSP00000422094.2:n.*1085G>A
ENST00000511527.5:c.1547G>A	ENSP00000420997.1:n.1547G>A
ENST00000514141.5:c.*1181G>A	ENSP00000423526.1:n.*1181G>A
NM_016218.2:c.2562G>A	NP_057302.1:p.Lys854=
XM_005248534.3:c.2604G>A	XP_005248591.1:p.Lys868=
XM_006714652.2:c.1317G>A	XP_006714715.1:p.Lys439=
XM_011543463.1:c.2604G>A	XP_011541765.1:p.Lys868=
XM_011543464.1:c.2604G>A	XP_011541766.1:p.Lys868=
XM_011543465.1:c.2604G>A	XP_011541767.1:p.Lys868=
XM_011543466.1:c.2604G>A	XP_011541768.1:p.Lys868=
XM_011543467.1:c.2334G>A	XP_011541769.1:p.Lys778=
XR_241784.1:n.2570G>A
XR_948273.1:n.2754G>A
NM_001345921.1:c.2364G>A	NP_001332850.1:p.Lys788=
NM_001345922.1:c.2292G>A	NP_001332851.1:p.Lys764=
NM_016218.3:c.2562G>A	NP_057302.1:p.Lys854=
NR_144315.1:n.2568G>A
XM_005248534.5:c.2604G>A	XP_005248591.1:p.Lys868=
XM_006714652.4:c.1317G>A	XP_006714715.1:p.Lys439=
XM_011543463.3:c.2604G>A	XP_011541765.1:p.Lys868=
XM_011543464.3:c.2604G>A	XP_011541766.1:p.Lys868=
XM_011543467.3:c.2334G>A	XP_011541769.1:p.Lys778=
XM_017009559.2:c.2562G>A	XP_016865048.1:p.Lys854=
XM_017009560.2:c.2562G>A	XP_016865049.1:p.Lys854=
XM_017009561.2:c.2406G>A	XP_016865050.1:p.Lys802=
XM_017009563.2:c.2292G>A	XP_016865052.1:p.Lys764=
XR_001742105.2:n.3052G>A
XR_001742107.2:n.3136G>A
XR_001742108.2:n.2670G>A
XR_241784.3:n.3094G>A
XR_948273.3:n.2754G>A
NM_001345921.2:c.2364G>A	NP_001332850.1:p.Lys788=
NM_001345922.2:c.2292G>A	NP_001332851.1:p.Lys764=
NM_001387110.2:c.2553G>A	NP_001374039.1:p.Lys851=
NM_001387111.2:c.2604G>A	NP_001374040.1:p.Lys868=
NM_001387113.2:c.2562G>A	NP_001374042.1:p.Lys854=
NM_016218.5:c.2562G>A	NP_057302.1:p.Lys854=
NR_144315.2:n.2427G>A
NR_170559.2:n.2416G>A
NR_170560.2:n.2648G>A
NM_001345921.3:c.2364G>A	NP_001332850.1:p.Lys788=
NM_001345922.3:c.2292G>A	NP_001332851.1:p.Lys764=
NM_001387110.3:c.2553G>A	NP_001374039.1:p.Lys851=
NM_001387111.3:c.2604G>A	NP_001374040.1:p.Lys868=
NM_001387113.3:c.2562G>A	NP_001374042.1:p.Lys854=
NM_001395893.1:c.2292G>A	NP_001382822.1:p.Lys764=
NM_001395894.1:c.2604G>A	NP_001382823.1:p.Lys868=
NM_001395897.1:c.2601G>A	NP_001382826.1:p.Lys867=
NM_001395899.1:c.2409G>A	NP_001382828.1:p.Lys803=
NM_001395900.1:c.2364G>A	NP_001382829.1:p.Lys788=
NM_001395901.1:c.2322G>A	NP_001382830.1:p.Lys774=
NM_001395902.1:c.2292G>A	NP_001382831.1:p.Lys764=
NM_016218.6:c.2562G>A MANE Select	NP_057302.1:p.Lys854=
NR_144315.3:n.2427G>A
NR_170559.3:n.2416G>A
NR_170560.3:n.2648G>A