Canonical Allele Identifier: CA2571228137
Gene: PKD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2116733_2116735del , CM000678.2:g.2116733_2116735del GRCh38
NC_000016.9:g.2166734_2166736del , CM000678.1:g.2166734_2166736del GRCh37
NC_000016.8:g.2106735_2106737del NCBI36
NG_008617.1:g.24168_24170del

Transcript Alleles

HGVS Amino-acid change
ENST00000262304.9:c.1607-87_1607-85del MANE Select ENSP00000262304.4:n.1607-87_1607-85del
ENST00000262304.8:c.1607-87_1607-85del ENSP00000262304.4:n.1607-87_1607-85del
ENST00000423118.5:c.1607-87_1607-85del ENSP00000399501.1:n.1607-87_1607-85del
ENST00000488185.2:c.472+758_472+760del
ENST00000568591.5:c.538-87_538-85del ENSP00000457162.1:n.538-87_538-85del
ENST00000570150.1:n.519-87_519-85del
NM_000296.3:c.1607-87_1607-85del NP_000287.3:n.1607-87_1607-85del
NM_001009944.2:c.1607-87_1607-85del NP_001009944.2:n.1607-87_1607-85del
XM_011522525.1:c.1661-87_1661-85del XP_011520827.1:n.1661-87_1661-85del
XM_011522526.1:c.1661-87_1661-85del XP_011520828.1:n.1661-87_1661-85del
XM_011522527.1:c.1661-87_1661-85del XP_011520829.1:n.1661-87_1661-85del
XM_011522528.1:c.1661-87_1661-85del XP_011520830.1:n.1661-87_1661-85del
XM_011522529.1:c.1661-87_1661-85del XP_011520831.1:n.1661-87_1661-85del
XM_011522530.1:c.1607-87_1607-85del XP_011520832.1:n.1607-87_1607-85del
XM_011522531.1:c.1589-87_1589-85del XP_011520833.1:n.1589-87_1589-85del
XM_011522532.1:c.1535-87_1535-85del XP_011520834.1:n.1535-87_1535-85del
XM_011522533.1:c.1454-87_1454-85del XP_011520835.1:n.1454-87_1454-85del
XM_011522534.1:c.1397-87_1397-85del XP_011520836.1:n.1397-87_1397-85del
XM_011522536.1:c.1661-87_1661-85del XP_011520838.1:n.1661-87_1661-85del
XR_932867.1:n.1676-87_1676-85del
XR_932868.1:n.1676-87_1676-85del
XR_932869.1:n.1676-87_1676-85del
XR_932870.1:n.1676-87_1676-85del
XM_011522528.3:c.1661-87_1661-85del XP_011520830.1:n.1661-87_1661-85del
XM_011522529.2:c.1661-87_1661-85del XP_011520831.1:n.1661-87_1661-85del
XM_024450298.1:c.1607-87_1607-85del XP_024306066.1:n.1607-87_1607-85del
XM_024450299.1:c.1535-87_1535-85del XP_024306067.1:n.1535-87_1535-85del
XM_024450300.1:c.1397-87_1397-85del XP_024306068.1:n.1397-87_1397-85del
NM_000296.4:c.1607-87_1607-85del NP_000287.4:n.1607-87_1607-85del
NM_001009944.3:c.1607-87_1607-85del MANE Select NP_001009944.3:n.1607-87_1607-85del