Canonical Allele Identifier: CA2202035670
Gene: PKD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2106667G= , CM000678.2:g.2106667G= GRCh38
NC_000016.9:g.2156668G= , CM000678.1:g.2156668G= GRCh37
NC_000016.8:g.2096669G= NCBI36
NG_008617.1:g.34232C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.7220C= MANE Select ENSP00000262304.4:p.Ala2407=
ENST00000262304.8:c.7220C= ENSP00000262304.4:p.Ala2407=
ENST00000415938.7:n.465C=
ENST00000423118.5:c.7220C= ENSP00000399501.1:p.Ala2407=
ENST00000483024.1:c.388C=
ENST00000483558.5:n.279C=
ENST00000483731.5:n.945C=
ENST00000486339.6:n.966C=
ENST00000487932.5:c.1907C= ENSP00000457132.1:p.Ala636=
ENST00000496574.6:n.1223C=
ENST00000565639.6:n.928C=
ENST00000568591.5:c.2381C= ENSP00000457162.1:n.2381C=
ENST00000569983.5:n.576C=
NM_000296.3:c.7220C= NP_000287.3:p.Ala2407=
NM_001009944.2:c.7220C= NP_001009944.2:p.Ala2407=
XM_005255370.2:c.4175C= XP_005255427.1:p.Ala1392=
XM_011522525.1:c.7298C= XP_011520827.1:p.Ala2433=
XM_011522526.1:c.7298C= XP_011520828.1:p.Ala2433=
XM_011522527.1:c.7298C= XP_011520829.1:p.Ala2433=
XM_011522528.1:c.7274C= XP_011520830.1:p.Ala2425=
XM_011522529.1:c.7274C= XP_011520831.1:p.Ala2425=
XM_011522530.1:c.7244C= XP_011520832.1:p.Ala2415=
XM_011522531.1:c.7226C= XP_011520833.1:p.Ala2409=
XM_011522532.1:c.7172C= XP_011520834.1:p.Ala2391=
XM_011522533.1:c.7091C= XP_011520835.1:p.Ala2364=
XM_011522534.1:c.7034C= XP_011520836.1:p.Ala2345=
XM_011522535.1:c.5120C= XP_011520837.1:p.Ala1707=
XM_011522536.1:c.7298C= XP_011520838.1:p.Ala2433=
XM_011522537.1:c.4298C= XP_011520839.1:p.Ala1433=
XR_932867.1:n.7313C=
XR_932868.1:n.7313C=
XR_932869.1:n.7313C=
XR_932870.1:n.7313C=
XM_005255370.3:c.4175C= XP_005255427.1:p.Ala1392=
XM_011522528.3:c.7274C= XP_011520830.1:p.Ala2425=
XM_011522529.2:c.7274C= XP_011520831.1:p.Ala2425=
XM_011522537.2:c.4298C= XP_011520839.1:p.Ala1433=
XM_024450298.1:c.7340C= XP_024306066.1:p.Ala2447=
XM_024450299.1:c.7268C= XP_024306067.1:p.Ala2423=
XM_024450300.1:c.7130C= XP_024306068.1:p.Ala2377=
XM_024450301.1:c.5216C= XP_024306069.1:p.Ala1739=
NM_000296.4:c.7220C= NP_000287.4:p.Ala2407=
NM_001009944.3:c.7220C= MANE Select NP_001009944.3:p.Ala2407=