Canonical Allele Identifier: CA394387415
Gene: PKD1 HGNC NCBI

Linked Data

dbSNP Id: rs2092595134
gnomAD v3: 16-2114436-C-T
gnomAD v4: 16-2114436-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2114436C>T , CM000678.2:g.2114436C>T GRCh38
NC_000016.9:g.2164437C>T , CM000678.1:g.2164437C>T GRCh37
NC_000016.8:g.2104438C>T NCBI36
NG_008617.1:g.26463G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.2587G>A MANE Select ENSP00000262304.4:p.Gly863Arg
ENST00000262304.8:c.2587G>A ENSP00000262304.4:p.Gly863Arg
ENST00000423118.5:c.2587G>A ENSP00000399501.1:p.Gly863Arg
ENST00000488185.2:c.472+3053G>A
ENST00000565639.6:n.46G>A
ENST00000568591.5:c.1518G>A ENSP00000457162.1:n.1518G>A
NM_000296.3:c.2587G>A NP_000287.3:p.Gly863Arg
NM_001009944.2:c.2587G>A NP_001009944.2:p.Gly863Arg
XM_011522525.1:c.2641G>A XP_011520827.1:p.Gly881Arg
XM_011522526.1:c.2641G>A XP_011520828.1:p.Gly881Arg
XM_011522527.1:c.2641G>A XP_011520829.1:p.Gly881Arg
XM_011522528.1:c.2641G>A XP_011520830.1:p.Gly881Arg
XM_011522529.1:c.2641G>A XP_011520831.1:p.Gly881Arg
XM_011522530.1:c.2587G>A XP_011520832.1:p.Gly863Arg
XM_011522531.1:c.2569G>A XP_011520833.1:p.Gly857Arg
XM_011522532.1:c.2515G>A XP_011520834.1:p.Gly839Arg
XM_011522533.1:c.2434G>A XP_011520835.1:p.Gly812Arg
XM_011522534.1:c.2377G>A XP_011520836.1:p.Gly793Arg
XM_011522535.1:c.463G>A XP_011520837.1:p.Gly155Arg
XM_011522536.1:c.2641G>A XP_011520838.1:p.Gly881Arg
XR_932867.1:n.2656G>A
XR_932868.1:n.2656G>A
XR_932869.1:n.2656G>A
XR_932870.1:n.2656G>A
XM_005255370.3:c.-463G>A XP_005255427.1:n.-463G>A
XM_011522528.3:c.2641G>A XP_011520830.1:p.Gly881Arg
XM_011522529.2:c.2641G>A XP_011520831.1:p.Gly881Arg
XM_024450298.1:c.2587G>A XP_024306066.1:p.Gly863Arg
XM_024450299.1:c.2515G>A XP_024306067.1:p.Gly839Arg
XM_024450300.1:c.2377G>A XP_024306068.1:p.Gly793Arg
XM_024450301.1:c.463G>A XP_024306069.1:p.Gly155Arg
NM_000296.4:c.2587G>A NP_000287.4:p.Gly863Arg
NM_001009944.3:c.2587G>A MANE Select NP_001009944.3:p.Gly863Arg