Canonical Allele Identifier: CA2695222584
Gene: PKD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2115461dup , CM000678.2:g.2115461dup GRCh38
NC_000016.9:g.2165462dup , CM000678.1:g.2165462dup GRCh37
NC_000016.8:g.2105463dup NCBI36
NG_008617.1:g.25440dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.2016dup MANE Select ENSP00000262304.4:p.Pro673AlafsTer?
ENST00000262304.8:c.2016dup ENSP00000262304.4:p.Pro673AlafsTer?
ENST00000423118.5:c.2016dup ENSP00000399501.1:p.Pro673AlafsTer?
ENST00000488185.2:c.472+2030dup
ENST00000568591.5:c.947dup ENSP00000457162.1:n.947dup
NM_000296.3:c.2016dup NP_000287.3:p.Pro673AlafsTer?
NM_001009944.2:c.2016dup NP_001009944.2:p.Pro673AlafsTer?
XM_011522525.1:c.2070dup XP_011520827.1:p.Pro691AlafsTer?
XM_011522526.1:c.2070dup XP_011520828.1:p.Pro691AlafsTer?
XM_011522527.1:c.2070dup XP_011520829.1:p.Pro691AlafsTer?
XM_011522528.1:c.2070dup XP_011520830.1:p.Pro691AlafsTer?
XM_011522529.1:c.2070dup XP_011520831.1:p.Pro691AlafsTer?
XM_011522530.1:c.2016dup XP_011520832.1:p.Pro673AlafsTer?
XM_011522531.1:c.1998dup XP_011520833.1:p.Pro667AlafsTer?
XM_011522532.1:c.1944dup XP_011520834.1:p.Pro649AlafsTer?
XM_011522533.1:c.1863dup XP_011520835.1:p.Pro622AlafsTer?
XM_011522534.1:c.1806dup XP_011520836.1:p.Pro603AlafsTer?
XM_011522536.1:c.2070dup XP_011520838.1:p.Pro691AlafsTer?
XR_932867.1:n.2085dup
XR_932868.1:n.2085dup
XR_932869.1:n.2085dup
XR_932870.1:n.2085dup
XM_011522528.3:c.2070dup XP_011520830.1:p.Pro691AlafsTer?
XM_011522529.2:c.2070dup XP_011520831.1:p.Pro691AlafsTer?
XM_024450298.1:c.2016dup XP_024306066.1:p.Pro673AlafsTer?
XM_024450299.1:c.1944dup XP_024306067.1:p.Pro649AlafsTer?
XM_024450300.1:c.1806dup XP_024306068.1:p.Pro603AlafsTer?
NM_000296.4:c.2016dup NP_000287.4:p.Pro673AlafsTer?
NM_001009944.3:c.2016dup MANE Select NP_001009944.3:p.Pro673AlafsTer?