Canonical Allele Identifier: CA2767051188

Gene: POLK

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.75597990_75597991insC , CM000667.2:g.75597990_75597991insC	GRCh38
NC_000005.9:g.74893815_74893816insC , CM000667.1:g.74893815_74893816insC	GRCh37
NC_000005.8:g.74929571_74929572insC	NCBI36
NG_051590.1:g.91241_91242insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000241436.9:c.2585_2586insC MANE Select	ENSP00000241436.4:p.Lys862AsnfsTer5
ENST00000241436.8:c.2585_2586insC	ENSP00000241436.4:p.Lys862AsnfsTer5
ENST00000503479.6:c.*1108_*1109insC	ENSP00000421997.2:n.*1108_*1109insC
ENST00000504026.5:c.1456_1457insC	ENSP00000425075.1:n.1456_1457insC
ENST00000505069.1:n.309_310insC
ENST00000505975.5:c.2699_2700insC	ENSP00000424859.1:n.2699_2700insC
ENST00000506928.5:n.2708_2709insC
ENST00000508526.5:c.1991_1992insC	ENSP00000426853.1:p.Lys664AsnfsTer5
ENST00000509126.2:c.2413_2414insC	ENSP00000423532.1:n.2413_2414insC
ENST00000510815.6:c.*1108_*1109insC	ENSP00000422094.2:n.*1108_*1109insC
ENST00000511527.5:c.1570_1571insC	ENSP00000420997.1:n.1570_1571insC
ENST00000514141.5:c.*1204_*1205insC	ENSP00000423526.1:n.*1204_*1205insC
NM_016218.2:c.2585_2586insC	NP_057302.1:p.Lys862AsnfsTer5
XM_005248534.3:c.2627_2628insC	XP_005248591.1:p.Lys876AsnfsTer5
XM_006714652.2:c.1340_1341insC	XP_006714715.1:p.Lys447AsnfsTer5
XM_011543463.1:c.2627_2628insC	XP_011541765.1:p.Lys876AsnfsTer5
XM_011543464.1:c.2627_2628insC	XP_011541766.1:p.Lys876AsnfsTer5
XM_011543465.1:c.2627_2628insC	XP_011541767.1:p.Lys876AsnfsTer5
XM_011543466.1:c.2627_2628insC	XP_011541768.1:p.Lys876AsnfsTer5
XM_011543467.1:c.2357_2358insC	XP_011541769.1:p.Lys786AsnfsTer5
XR_241784.1:n.2593_2594insC
XR_948273.1:n.2777_2778insC
NM_001345921.1:c.2387_2388insC	NP_001332850.1:p.Lys796AsnfsTer5
NM_001345922.1:c.2315_2316insC	NP_001332851.1:p.Lys772AsnfsTer5
NM_016218.3:c.2585_2586insC	NP_057302.1:p.Lys862AsnfsTer5
NR_144315.1:n.2591_2592insC
XM_005248534.5:c.2627_2628insC	XP_005248591.1:p.Lys876AsnfsTer5
XM_006714652.4:c.1340_1341insC	XP_006714715.1:p.Lys447AsnfsTer5
XM_011543463.3:c.2627_2628insC	XP_011541765.1:p.Lys876AsnfsTer5
XM_011543464.3:c.2627_2628insC	XP_011541766.1:p.Lys876AsnfsTer5
XM_011543467.3:c.2357_2358insC	XP_011541769.1:p.Lys786AsnfsTer5
XM_017009559.2:c.2585_2586insC	XP_016865048.1:p.Lys862AsnfsTer5
XM_017009560.2:c.2585_2586insC	XP_016865049.1:p.Lys862AsnfsTer5
XM_017009561.2:c.2429_2430insC	XP_016865050.1:p.Lys810AsnfsTer5
XM_017009563.2:c.2315_2316insC	XP_016865052.1:p.Lys772AsnfsTer5
XR_001742105.2:n.3075_3076insC
XR_001742107.2:n.3159_3160insC
XR_001742108.2:n.2693_2694insC
XR_241784.3:n.3117_3118insC
XR_948273.3:n.2777_2778insC
NM_001345921.2:c.2387_2388insC	NP_001332850.1:p.Lys796AsnfsTer5
NM_001345922.2:c.2315_2316insC	NP_001332851.1:p.Lys772AsnfsTer5
NM_001387110.2:c.2576_2577insC	NP_001374039.1:p.Lys859AsnfsTer5
NM_001387111.2:c.2627_2628insC	NP_001374040.1:p.Lys876AsnfsTer5
NM_001387113.2:c.2585_2586insC	NP_001374042.1:p.Lys862AsnfsTer5
NM_016218.5:c.2585_2586insC	NP_057302.1:p.Lys862AsnfsTer5
NR_144315.2:n.2450_2451insC
NR_170559.2:n.2439_2440insC
NR_170560.2:n.2671_2672insC
NM_001345921.3:c.2387_2388insC	NP_001332850.1:p.Lys796AsnfsTer5
NM_001345922.3:c.2315_2316insC	NP_001332851.1:p.Lys772AsnfsTer5
NM_001387110.3:c.2576_2577insC	NP_001374039.1:p.Lys859AsnfsTer5
NM_001387111.3:c.2627_2628insC	NP_001374040.1:p.Lys876AsnfsTer5
NM_001387113.3:c.2585_2586insC	NP_001374042.1:p.Lys862AsnfsTer5
NM_001395893.1:c.2315_2316insC	NP_001382822.1:p.Lys772AsnfsTer5
NM_001395894.1:c.2627_2628insC	NP_001382823.1:p.Lys876AsnfsTer5
NM_001395897.1:c.2624_2625insC	NP_001382826.1:p.Lys875AsnfsTer5
NM_001395899.1:c.2432_2433insC	NP_001382828.1:p.Lys811AsnfsTer5
NM_001395900.1:c.2387_2388insC	NP_001382829.1:p.Lys796AsnfsTer5
NM_001395901.1:c.2345_2346insC	NP_001382830.1:p.Lys782AsnfsTer5
NM_001395902.1:c.2315_2316insC	NP_001382831.1:p.Lys772AsnfsTer5
NM_016218.6:c.2585_2586insC MANE Select	NP_057302.1:p.Lys862AsnfsTer5
NR_144315.3:n.2450_2451insC
NR_170559.3:n.2439_2440insC
NR_170560.3:n.2671_2672insC