Canonical Allele Identifier: CA2202034969
Gene: PKD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2106556T= , CM000678.2:g.2106556T= GRCh38
NC_000016.9:g.2156557T= , CM000678.1:g.2156557T= GRCh37
NC_000016.8:g.2096558T= NCBI36
NG_008617.1:g.34343A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.7331A= MANE Select ENSP00000262304.4:p.Tyr2444=
ENST00000262304.8:c.7331A= ENSP00000262304.4:p.Tyr2444=
ENST00000415938.7:n.576A=
ENST00000423118.5:c.7331A= ENSP00000399501.1:p.Tyr2444=
ENST00000483558.5:n.390A=
ENST00000483731.5:n.1056A=
ENST00000486339.6:n.1077A=
ENST00000487932.5:c.2018A= ENSP00000457132.1:p.Tyr673=
ENST00000496574.6:n.1334A=
ENST00000565639.6:n.1039A=
ENST00000568591.5:c.2492A= ENSP00000457162.1:n.2492A=
ENST00000569983.5:n.687A=
NM_000296.3:c.7331A= NP_000287.3:p.Tyr2444=
NM_001009944.2:c.7331A= NP_001009944.2:p.Tyr2444=
XM_005255370.2:c.4286A= XP_005255427.1:p.Tyr1429=
XM_011522525.1:c.7409A= XP_011520827.1:p.Tyr2470=
XM_011522526.1:c.7409A= XP_011520828.1:p.Tyr2470=
XM_011522527.1:c.7409A= XP_011520829.1:p.Tyr2470=
XM_011522528.1:c.7385A= XP_011520830.1:p.Tyr2462=
XM_011522529.1:c.7385A= XP_011520831.1:p.Tyr2462=
XM_011522530.1:c.7355A= XP_011520832.1:p.Tyr2452=
XM_011522531.1:c.7337A= XP_011520833.1:p.Tyr2446=
XM_011522532.1:c.7283A= XP_011520834.1:p.Tyr2428=
XM_011522533.1:c.7202A= XP_011520835.1:p.Tyr2401=
XM_011522534.1:c.7145A= XP_011520836.1:p.Tyr2382=
XM_011522535.1:c.5231A= XP_011520837.1:p.Tyr1744=
XM_011522536.1:c.7409A= XP_011520838.1:p.Tyr2470=
XM_011522537.1:c.4409A= XP_011520839.1:p.Tyr1470=
XR_932867.1:n.7424A=
XR_932868.1:n.7424A=
XR_932869.1:n.7424A=
XR_932870.1:n.7424A=
XM_005255370.3:c.4286A= XP_005255427.1:p.Tyr1429=
XM_011522528.3:c.7385A= XP_011520830.1:p.Tyr2462=
XM_011522529.2:c.7385A= XP_011520831.1:p.Tyr2462=
XM_011522537.2:c.4409A= XP_011520839.1:p.Tyr1470=
XM_024450298.1:c.7451A= XP_024306066.1:p.Tyr2484=
XM_024450299.1:c.7379A= XP_024306067.1:p.Tyr2460=
XM_024450300.1:c.7241A= XP_024306068.1:p.Tyr2414=
XM_024450301.1:c.5327A= XP_024306069.1:p.Tyr1776=
NM_000296.4:c.7331A= NP_000287.4:p.Tyr2444=
NM_001009944.3:c.7331A= MANE Select NP_001009944.3:p.Tyr2444=