Canonical Allele Identifier: CA620705837
Gene: PKD1 HGNC NCBI

Linked Data

dbSNP Id: rs1567212593

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2115409_2115411del , CM000678.2:g.2115409_2115411del GRCh38
NC_000016.9:g.2165410_2165412del , CM000678.1:g.2165410_2165412del GRCh37
NC_000016.8:g.2105411_2105413del NCBI36
NG_008617.1:g.25489_25491del

Transcript Alleles

HGVS Amino-acid change
ENST00000262304.9:c.2065_2067del MANE Select ENSP00000262304.4:p.Ser689del
ENST00000262304.8:c.2065_2067del ENSP00000262304.4:p.Ser689del
ENST00000423118.5:c.2065_2067del ENSP00000399501.1:p.Ser689del
ENST00000488185.2:c.472+2079_472+2081del
ENST00000568591.5:c.996_998del ENSP00000457162.1:n.996_998del
NM_000296.3:c.2065_2067del NP_000287.3:p.Ser689del
NM_001009944.2:c.2065_2067del NP_001009944.2:p.Ser689del
XM_011522525.1:c.2119_2121del XP_011520827.1:p.Ser707del
XM_011522526.1:c.2119_2121del XP_011520828.1:p.Ser707del
XM_011522527.1:c.2119_2121del XP_011520829.1:p.Ser707del
XM_011522528.1:c.2119_2121del XP_011520830.1:p.Ser707del
XM_011522529.1:c.2119_2121del XP_011520831.1:p.Ser707del
XM_011522530.1:c.2065_2067del XP_011520832.1:p.Ser689del
XM_011522531.1:c.2047_2049del XP_011520833.1:p.Ser683del
XM_011522532.1:c.1993_1995del XP_011520834.1:p.Ser665del
XM_011522533.1:c.1912_1914del XP_011520835.1:p.Ser638del
XM_011522534.1:c.1855_1857del XP_011520836.1:p.Ser619del
XM_011522536.1:c.2119_2121del XP_011520838.1:p.Ser707del
XR_932867.1:n.2134_2136del
XR_932868.1:n.2134_2136del
XR_932869.1:n.2134_2136del
XR_932870.1:n.2134_2136del
XM_011522528.3:c.2119_2121del XP_011520830.1:p.Ser707del
XM_011522529.2:c.2119_2121del XP_011520831.1:p.Ser707del
XM_024450298.1:c.2065_2067del XP_024306066.1:p.Ser689del
XM_024450299.1:c.1993_1995del XP_024306067.1:p.Ser665del
XM_024450300.1:c.1855_1857del XP_024306068.1:p.Ser619del
NM_000296.4:c.2065_2067del NP_000287.4:p.Ser689del
NM_001009944.3:c.2065_2067del MANE Select NP_001009944.3:p.Ser689del