Canonical Allele Identifier: CA2202047665

Gene: PKD1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2111546_2111566delinsGCGCACATCCGCCTGGGCCGC , CM000678.2:g.2111546_2111566delinsGCGCACATCCGCCTGGGCCGC	GRCh38
NC_000016.9:g.2161547_2161567delinsGCGCACATCCGCCTGGGCCGC , CM000678.1:g.2161547_2161567delinsGCGCACATCCGCCTGGGCCGC	GRCh37
NC_000016.8:g.2101548_2101568delinsGCGCACATCCGCCTGGGCCGC	NCBI36
NG_008617.1:g.29333_29353delinsGCGGCCCAGGCGGATGTGCGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.3601_3621delinsGCGGCCCAGGCGGATGTGCGC MANE Select	ENSP00000262304.4:p.Ala1201=
ENST00000262304.8:c.3601_3621delinsGCGGCCCAGGCGGATGTGCGC	ENSP00000262304.4:p.Ala1201=
ENST00000415938.7:n.310+774_310+794delinsGCGGCCCAGGCGGATGTGCGC
ENST00000423118.5:c.3601_3621delinsGCGGCCCAGGCGGATGTGCGC	ENSP00000399501.1:p.Ala1201=
ENST00000468674.5:n.430+774_430+794delinsGCGGCCCAGGCGGATGTGCGC
ENST00000469241.2:n.551_571delinsGCGGCCCAGGCGGATGTGCGC
ENST00000483024.1:c.233+250_233+270delinsGCGGCCCAGGCGGATGTGCGC
ENST00000483731.5:n.790+774_790+794delinsGCGGCCCAGGCGGATGTGCGC
ENST00000488185.2:c.473-3208_473-3188delinsGCGGCCCAGGCGGATGTGCGC
ENST00000565639.6:n.773+774_773+794delinsGCGGCCCAGGCGGATGTGCGC
ENST00000568591.5:c.2226+774_2226+794delinsGCGGCCCAGGCGGATGTGCGC	ENSP00000457162.1:n.2226+774_2226+794delinsGCGGCCCAGGCGGATGTG...
ENST00000569983.5:n.421+774_421+794delinsGCGGCCCAGGCGGATGTGCGC
NM_000296.3:c.3601_3621delinsGCGGCCCAGGCGGATGTGCGC	NP_000287.3:p.Ala1201=
NM_001009944.2:c.3601_3621delinsGCGGCCCAGGCGGATGTGCGC	NP_001009944.2:p.Ala1201=
XM_005255370.2:c.556_576delinsGCGGCCCAGGCGGATGTGCGC	XP_005255427.1:p.Ala186=
XM_011522525.1:c.3679_3699delinsGCGGCCCAGGCGGATGTGCGC	XP_011520827.1:p.Ala1227=
XM_011522526.1:c.3679_3699delinsGCGGCCCAGGCGGATGTGCGC	XP_011520828.1:p.Ala1227=
XM_011522527.1:c.3679_3699delinsGCGGCCCAGGCGGATGTGCGC	XP_011520829.1:p.Ala1227=
XM_011522528.1:c.3655_3675delinsGCGGCCCAGGCGGATGTGCGC	XP_011520830.1:p.Ala1219=
XM_011522529.1:c.3655_3675delinsGCGGCCCAGGCGGATGTGCGC	XP_011520831.1:p.Ala1219=
XM_011522530.1:c.3625_3645delinsGCGGCCCAGGCGGATGTGCGC	XP_011520832.1:p.Ala1209=
XM_011522531.1:c.3607_3627delinsGCGGCCCAGGCGGATGTGCGC	XP_011520833.1:p.Ala1203=
XM_011522532.1:c.3553_3573delinsGCGGCCCAGGCGGATGTGCGC	XP_011520834.1:p.Ala1185=
XM_011522533.1:c.3472_3492delinsGCGGCCCAGGCGGATGTGCGC	XP_011520835.1:p.Ala1158=
XM_011522534.1:c.3415_3435delinsGCGGCCCAGGCGGATGTGCGC	XP_011520836.1:p.Ala1139=
XM_011522535.1:c.1501_1521delinsGCGGCCCAGGCGGATGTGCGC	XP_011520837.1:p.Ala501=
XM_011522536.1:c.3679_3699delinsGCGGCCCAGGCGGATGTGCGC	XP_011520838.1:p.Ala1227=
XM_011522537.1:c.679_699delinsGCGGCCCAGGCGGATGTGCGC	XP_011520839.1:p.Ala227=
XR_932867.1:n.3694_3714delinsGCGGCCCAGGCGGATGTGCGC
XR_932868.1:n.3694_3714delinsGCGGCCCAGGCGGATGTGCGC
XR_932869.1:n.3694_3714delinsGCGGCCCAGGCGGATGTGCGC
XR_932870.1:n.3694_3714delinsGCGGCCCAGGCGGATGTGCGC
XM_005255370.3:c.556_576delinsGCGGCCCAGGCGGATGTGCGC	XP_005255427.1:p.Ala186=
XM_011522528.3:c.3655_3675delinsGCGGCCCAGGCGGATGTGCGC	XP_011520830.1:p.Ala1219=
XM_011522529.2:c.3655_3675delinsGCGGCCCAGGCGGATGTGCGC	XP_011520831.1:p.Ala1219=
XM_011522537.2:c.679_699delinsGCGGCCCAGGCGGATGTGCGC	XP_011520839.1:p.Ala227=
XM_024450298.1:c.3721_3741delinsGCGGCCCAGGCGGATGTGCGC	XP_024306066.1:p.Ala1241=
XM_024450299.1:c.3649_3669delinsGCGGCCCAGGCGGATGTGCGC	XP_024306067.1:p.Ala1217=
XM_024450300.1:c.3511_3531delinsGCGGCCCAGGCGGATGTGCGC	XP_024306068.1:p.Ala1171=
XM_024450301.1:c.1597_1617delinsGCGGCCCAGGCGGATGTGCGC	XP_024306069.1:p.Ala533=
NM_000296.4:c.3601_3621delinsGCGGCCCAGGCGGATGTGCGC	NP_000287.4:p.Ala1201=
NM_001009944.3:c.3601_3621delinsGCGGCCCAGGCGGATGTGCGC MANE Select	NP_001009944.3:p.Ala1201=