Canonical Allele Identifier: CA358180
Gene: PKD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 225056
dbSNP Id: rs869312944

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2100402_2100404del , CM000678.2:g.2100402_2100404del GRCh38
NC_000016.9:g.2150403_2150405del , CM000678.1:g.2150403_2150405del GRCh37
NC_000016.8:g.2090404_2090406del NCBI36
NG_008617.1:g.42821_42823del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.9564_9566del MANE Select ENSP00000262304.4:p.Asn3188del
ENST00000262304.8:c.9564_9566del ENSP00000262304.4:p.Asn3188del
ENST00000415938.7:n.2643_2645del
ENST00000423118.5:c.9564_9566del ENSP00000399501.1:p.Asn3188del
ENST00000469851.1:n.287_289del
ENST00000471603.6:n.1208_1210del
ENST00000480227.5:n.1301_1303del
ENST00000483731.5:n.3450_3452del
ENST00000483814.1:n.366_368del
ENST00000486339.6:n.3700_3702del
ENST00000487932.5:c.4126_4128del ENSP00000457132.1:n.4126_4128del
ENST00000496574.6:n.3800_3802del
ENST00000562297.5:n.1297_1299del
ENST00000566905.5:n.54_56del
ENST00000567946.1:c.1166_1168del
ENST00000570193.5:n.8_10del
NM_000296.3:c.9564_9566del NP_000287.3:p.Asn3188del
NM_001009944.2:c.9564_9566del NP_001009944.2:p.Asn3188del
XM_005255370.2:c.6519_6521del XP_005255427.1:p.Asn2173del
XM_011522525.1:c.9642_9644del XP_011520827.1:p.Asn3214del
XM_011522526.1:c.9642_9644del XP_011520828.1:p.Asn3214del
XM_011522527.1:c.9624_9626del XP_011520829.1:p.Asn3208del
XM_011522528.1:c.9618_9620del XP_011520830.1:p.Asn3206del
XM_011522529.1:c.9618_9620del XP_011520831.1:p.Asn3206del
XM_011522530.1:c.9588_9590del XP_011520832.1:p.Asn3196del
XM_011522531.1:c.9570_9572del XP_011520833.1:p.Asn3190del
XM_011522532.1:c.9516_9518del XP_011520834.1:p.Asn3172del
XM_011522533.1:c.9435_9437del XP_011520835.1:p.Asn3145del
XM_011522534.1:c.9378_9380del XP_011520836.1:p.Asn3126del
XM_011522535.1:c.7464_7466del XP_011520837.1:p.Asn2488del
XM_011522536.1:c.9642_9644del XP_011520838.1:p.Asn3214del
XM_011522537.1:c.6642_6644del XP_011520839.1:p.Asn2214del
XR_932867.1:n.9657_9659del
XR_932868.1:n.9657_9659del
XR_932869.1:n.9657_9659del
XR_932870.1:n.9657_9659del
XM_005255370.3:c.6519_6521del XP_005255427.1:p.Asn2173del
XM_011522528.3:c.9618_9620del XP_011520830.1:p.Asn3206del
XM_011522529.2:c.9618_9620del XP_011520831.1:p.Asn3206del
XM_011522537.2:c.6642_6644del XP_011520839.1:p.Asn2214del
XM_024450298.1:c.9684_9686del XP_024306066.1:p.Asn3228del
XM_024450299.1:c.9612_9614del XP_024306067.1:p.Asn3204del
XM_024450300.1:c.9474_9476del XP_024306068.1:p.Asn3158del
XM_024450301.1:c.7560_7562del XP_024306069.1:p.Asn2520del
NM_000296.4:c.9564_9566del NP_000287.4:p.Asn3188del
NM_001009944.3:c.9564_9566del MANE Select NP_001009944.3:p.Asn3188del