Canonical Allele Identifier: CA2202047780
Gene: PKD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2111704C= , CM000678.2:g.2111704C= GRCh38
NC_000016.9:g.2161705C= , CM000678.1:g.2161705C= GRCh37
NC_000016.8:g.2101706C= NCBI36
NG_008617.1:g.29195G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.3463G= MANE Select ENSP00000262304.4:p.Gly1155=
ENST00000262304.8:c.3463G= ENSP00000262304.4:p.Gly1155=
ENST00000415938.7:n.310+636G=
ENST00000423118.5:c.3463G= ENSP00000399501.1:p.Gly1155=
ENST00000468674.5:n.430+636G=
ENST00000469241.2:n.413G=
ENST00000483024.1:c.233+112G=
ENST00000483731.5:n.790+636G=
ENST00000488185.2:c.473-3346G=
ENST00000565639.6:n.773+636G=
ENST00000568591.5:c.2226+636G= ENSP00000457162.1:n.2226+636G=
ENST00000569983.5:n.421+636G=
NM_000296.3:c.3463G= NP_000287.3:p.Gly1155=
NM_001009944.2:c.3463G= NP_001009944.2:p.Gly1155=
XM_005255370.2:c.418G= XP_005255427.1:p.Gly140=
XM_011522525.1:c.3541G= XP_011520827.1:p.Gly1181=
XM_011522526.1:c.3541G= XP_011520828.1:p.Gly1181=
XM_011522527.1:c.3541G= XP_011520829.1:p.Gly1181=
XM_011522528.1:c.3517G= XP_011520830.1:p.Gly1173=
XM_011522529.1:c.3517G= XP_011520831.1:p.Gly1173=
XM_011522530.1:c.3487G= XP_011520832.1:p.Gly1163=
XM_011522531.1:c.3469G= XP_011520833.1:p.Gly1157=
XM_011522532.1:c.3415G= XP_011520834.1:p.Gly1139=
XM_011522533.1:c.3334G= XP_011520835.1:p.Gly1112=
XM_011522534.1:c.3277G= XP_011520836.1:p.Gly1093=
XM_011522535.1:c.1363G= XP_011520837.1:p.Gly455=
XM_011522536.1:c.3541G= XP_011520838.1:p.Gly1181=
XM_011522537.1:c.541G= XP_011520839.1:p.Gly181=
XR_932867.1:n.3556G=
XR_932868.1:n.3556G=
XR_932869.1:n.3556G=
XR_932870.1:n.3556G=
XM_005255370.3:c.418G= XP_005255427.1:p.Gly140=
XM_011522528.3:c.3517G= XP_011520830.1:p.Gly1173=
XM_011522529.2:c.3517G= XP_011520831.1:p.Gly1173=
XM_011522537.2:c.541G= XP_011520839.1:p.Gly181=
XM_024450298.1:c.3583G= XP_024306066.1:p.Gly1195=
XM_024450299.1:c.3511G= XP_024306067.1:p.Gly1171=
XM_024450300.1:c.3373G= XP_024306068.1:p.Gly1125=
XM_024450301.1:c.1459G= XP_024306069.1:p.Gly487=
NM_000296.4:c.3463G= NP_000287.4:p.Gly1155=
NM_001009944.3:c.3463G= MANE Select NP_001009944.3:p.Gly1155=