Canonical Allele Identifier: CA2202047688
Gene: PKD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2111573G= , CM000678.2:g.2111573G= GRCh38
NC_000016.9:g.2161574G= , CM000678.1:g.2161574G= GRCh37
NC_000016.8:g.2101575G= NCBI36
NG_008617.1:g.29326C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.3594C= MANE Select ENSP00000262304.4:p.Ser1198=
ENST00000262304.8:c.3594C= ENSP00000262304.4:p.Ser1198=
ENST00000415938.7:n.310+767C=
ENST00000423118.5:c.3594C= ENSP00000399501.1:p.Ser1198=
ENST00000468674.5:n.430+767C=
ENST00000469241.2:n.544C=
ENST00000483024.1:c.233+243C=
ENST00000483731.5:n.790+767C=
ENST00000488185.2:c.473-3215C=
ENST00000565639.6:n.773+767C=
ENST00000568591.5:c.2226+767C= ENSP00000457162.1:n.2226+767C=
ENST00000569983.5:n.421+767C=
NM_000296.3:c.3594C= NP_000287.3:p.Ser1198=
NM_001009944.2:c.3594C= NP_001009944.2:p.Ser1198=
XM_005255370.2:c.549C= XP_005255427.1:p.Ser183=
XM_011522525.1:c.3672C= XP_011520827.1:p.Ser1224=
XM_011522526.1:c.3672C= XP_011520828.1:p.Ser1224=
XM_011522527.1:c.3672C= XP_011520829.1:p.Ser1224=
XM_011522528.1:c.3648C= XP_011520830.1:p.Ser1216=
XM_011522529.1:c.3648C= XP_011520831.1:p.Ser1216=
XM_011522530.1:c.3618C= XP_011520832.1:p.Ser1206=
XM_011522531.1:c.3600C= XP_011520833.1:p.Ser1200=
XM_011522532.1:c.3546C= XP_011520834.1:p.Ser1182=
XM_011522533.1:c.3465C= XP_011520835.1:p.Ser1155=
XM_011522534.1:c.3408C= XP_011520836.1:p.Ser1136=
XM_011522535.1:c.1494C= XP_011520837.1:p.Ser498=
XM_011522536.1:c.3672C= XP_011520838.1:p.Ser1224=
XM_011522537.1:c.672C= XP_011520839.1:p.Ser224=
XR_932867.1:n.3687C=
XR_932868.1:n.3687C=
XR_932869.1:n.3687C=
XR_932870.1:n.3687C=
XM_005255370.3:c.549C= XP_005255427.1:p.Ser183=
XM_011522528.3:c.3648C= XP_011520830.1:p.Ser1216=
XM_011522529.2:c.3648C= XP_011520831.1:p.Ser1216=
XM_011522537.2:c.672C= XP_011520839.1:p.Ser224=
XM_024450298.1:c.3714C= XP_024306066.1:p.Ser1238=
XM_024450299.1:c.3642C= XP_024306067.1:p.Ser1214=
XM_024450300.1:c.3504C= XP_024306068.1:p.Ser1168=
XM_024450301.1:c.1590C= XP_024306069.1:p.Ser530=
NM_000296.4:c.3594C= NP_000287.4:p.Ser1198=
NM_001009944.3:c.3594C= MANE Select NP_001009944.3:p.Ser1198=