Canonical Allele Identifier: CA394387360
Gene: PKD1 HGNC NCBI

Linked Data

dbSNP Id: rs189095400
gnomAD v2: 16-2164419-G-C
gnomAD v4: 16-2114418-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2114418G>C , CM000678.2:g.2114418G>C GRCh38
NC_000016.9:g.2164419G>C , CM000678.1:g.2164419G>C GRCh37
NC_000016.8:g.2104420G>C NCBI36
NG_008617.1:g.26481C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.2605C>G MANE Select ENSP00000262304.4:p.Arg869Gly
ENST00000262304.8:c.2605C>G ENSP00000262304.4:p.Arg869Gly
ENST00000423118.5:c.2605C>G ENSP00000399501.1:p.Arg869Gly
ENST00000488185.2:c.472+3071C>G
ENST00000565639.6:n.64C>G
ENST00000568591.5:c.1536C>G ENSP00000457162.1:n.1536C>G
NM_000296.3:c.2605C>G NP_000287.3:p.Arg869Gly
NM_001009944.2:c.2605C>G NP_001009944.2:p.Arg869Gly
XM_011522525.1:c.2659C>G XP_011520827.1:p.Arg887Gly
XM_011522526.1:c.2659C>G XP_011520828.1:p.Arg887Gly
XM_011522527.1:c.2659C>G XP_011520829.1:p.Arg887Gly
XM_011522528.1:c.2659C>G XP_011520830.1:p.Arg887Gly
XM_011522529.1:c.2659C>G XP_011520831.1:p.Arg887Gly
XM_011522530.1:c.2605C>G XP_011520832.1:p.Arg869Gly
XM_011522531.1:c.2587C>G XP_011520833.1:p.Arg863Gly
XM_011522532.1:c.2533C>G XP_011520834.1:p.Arg845Gly
XM_011522533.1:c.2452C>G XP_011520835.1:p.Arg818Gly
XM_011522534.1:c.2395C>G XP_011520836.1:p.Arg799Gly
XM_011522535.1:c.481C>G XP_011520837.1:p.Arg161Gly
XM_011522536.1:c.2659C>G XP_011520838.1:p.Arg887Gly
XR_932867.1:n.2674C>G
XR_932868.1:n.2674C>G
XR_932869.1:n.2674C>G
XR_932870.1:n.2674C>G
XM_005255370.3:c.-445C>G XP_005255427.1:n.-445C>G
XM_011522528.3:c.2659C>G XP_011520830.1:p.Arg887Gly
XM_011522529.2:c.2659C>G XP_011520831.1:p.Arg887Gly
XM_024450298.1:c.2605C>G XP_024306066.1:p.Arg869Gly
XM_024450299.1:c.2533C>G XP_024306067.1:p.Arg845Gly
XM_024450300.1:c.2395C>G XP_024306068.1:p.Arg799Gly
XM_024450301.1:c.481C>G XP_024306069.1:p.Arg161Gly
NM_000296.4:c.2605C>G NP_000287.4:p.Arg869Gly
NM_001009944.3:c.2605C>G MANE Select NP_001009944.3:p.Arg869Gly