Canonical Allele Identifier: CA2575879123
Gene: PKD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2115214_2115215del , CM000678.2:g.2115214_2115215del GRCh38
NC_000016.9:g.2165215_2165216del , CM000678.1:g.2165215_2165216del GRCh37
NC_000016.8:g.2105216_2105217del NCBI36
NG_008617.1:g.25685_25686del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.2097+164_2097+165del MANE Select ENSP00000262304.4:n.2097+164_2097+165del
ENST00000262304.8:c.2097+164_2097+165del ENSP00000262304.4:n.2097+164_2097+165del
ENST00000423118.5:c.2097+164_2097+165del ENSP00000399501.1:n.2097+164_2097+165del
ENST00000488185.2:c.472+2275_472+2276del
ENST00000568591.5:c.1028+164_1028+165del ENSP00000457162.1:n.1028+164_1028+165del
NM_000296.3:c.2097+164_2097+165del NP_000287.3:n.2097+164_2097+165del
NM_001009944.2:c.2097+164_2097+165del NP_001009944.2:n.2097+164_2097+165del
XM_011522525.1:c.2151+164_2151+165del XP_011520827.1:n.2151+164_2151+165del
XM_011522526.1:c.2151+164_2151+165del XP_011520828.1:n.2151+164_2151+165del
XM_011522527.1:c.2151+164_2151+165del XP_011520829.1:n.2151+164_2151+165del
XM_011522528.1:c.2151+164_2151+165del XP_011520830.1:n.2151+164_2151+165del
XM_011522529.1:c.2151+164_2151+165del XP_011520831.1:n.2151+164_2151+165del
XM_011522530.1:c.2097+164_2097+165del XP_011520832.1:n.2097+164_2097+165del
XM_011522531.1:c.2079+164_2079+165del XP_011520833.1:n.2079+164_2079+165del
XM_011522532.1:c.2025+164_2025+165del XP_011520834.1:n.2025+164_2025+165del
XM_011522533.1:c.1944+164_1944+165del XP_011520835.1:n.1944+164_1944+165del
XM_011522534.1:c.1887+164_1887+165del XP_011520836.1:n.1887+164_1887+165del
XM_011522535.1:c.-207_-206del XP_011520837.1:n.-207_-206del
XM_011522536.1:c.2151+164_2151+165del XP_011520838.1:n.2151+164_2151+165del
XR_932867.1:n.2166+164_2166+165del
XR_932868.1:n.2166+164_2166+165del
XR_932869.1:n.2166+164_2166+165del
XR_932870.1:n.2166+164_2166+165del
XM_011522528.3:c.2151+164_2151+165del XP_011520830.1:n.2151+164_2151+165del
XM_011522529.2:c.2151+164_2151+165del XP_011520831.1:n.2151+164_2151+165del
XM_024450298.1:c.2097+164_2097+165del XP_024306066.1:n.2097+164_2097+165del
XM_024450299.1:c.2025+164_2025+165del XP_024306067.1:n.2025+164_2025+165del
XM_024450300.1:c.1887+164_1887+165del XP_024306068.1:n.1887+164_1887+165del
XM_024450301.1:c.-207_-206del XP_024306069.1:n.-207_-206del
NM_000296.4:c.2097+164_2097+165del NP_000287.4:n.2097+164_2097+165del
NM_001009944.3:c.2097+164_2097+165del MANE Select NP_001009944.3:n.2097+164_2097+165del