Canonical Allele Identifier: CA2202035265
Gene: PKD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2106598C= , CM000678.2:g.2106598C= GRCh38
NC_000016.9:g.2156599C= , CM000678.1:g.2156599C= GRCh37
NC_000016.8:g.2096600C= NCBI36
NG_008617.1:g.34301G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.7289G= MANE Select ENSP00000262304.4:p.Arg2430=
ENST00000262304.8:c.7289G= ENSP00000262304.4:p.Arg2430=
ENST00000415938.7:n.534G=
ENST00000423118.5:c.7289G= ENSP00000399501.1:p.Arg2430=
ENST00000483024.1:c.457G=
ENST00000483558.5:n.348G=
ENST00000483731.5:n.1014G=
ENST00000486339.6:n.1035G=
ENST00000487932.5:c.1976G= ENSP00000457132.1:p.Arg659=
ENST00000496574.6:n.1292G=
ENST00000565639.6:n.997G=
ENST00000568591.5:c.2450G= ENSP00000457162.1:n.2450G=
ENST00000569983.5:n.645G=
NM_000296.3:c.7289G= NP_000287.3:p.Arg2430=
NM_001009944.2:c.7289G= NP_001009944.2:p.Arg2430=
XM_005255370.2:c.4244G= XP_005255427.1:p.Arg1415=
XM_011522525.1:c.7367G= XP_011520827.1:p.Arg2456=
XM_011522526.1:c.7367G= XP_011520828.1:p.Arg2456=
XM_011522527.1:c.7367G= XP_011520829.1:p.Arg2456=
XM_011522528.1:c.7343G= XP_011520830.1:p.Arg2448=
XM_011522529.1:c.7343G= XP_011520831.1:p.Arg2448=
XM_011522530.1:c.7313G= XP_011520832.1:p.Arg2438=
XM_011522531.1:c.7295G= XP_011520833.1:p.Arg2432=
XM_011522532.1:c.7241G= XP_011520834.1:p.Arg2414=
XM_011522533.1:c.7160G= XP_011520835.1:p.Arg2387=
XM_011522534.1:c.7103G= XP_011520836.1:p.Arg2368=
XM_011522535.1:c.5189G= XP_011520837.1:p.Arg1730=
XM_011522536.1:c.7367G= XP_011520838.1:p.Arg2456=
XM_011522537.1:c.4367G= XP_011520839.1:p.Arg1456=
XR_932867.1:n.7382G=
XR_932868.1:n.7382G=
XR_932869.1:n.7382G=
XR_932870.1:n.7382G=
XM_005255370.3:c.4244G= XP_005255427.1:p.Arg1415=
XM_011522528.3:c.7343G= XP_011520830.1:p.Arg2448=
XM_011522529.2:c.7343G= XP_011520831.1:p.Arg2448=
XM_011522537.2:c.4367G= XP_011520839.1:p.Arg1456=
XM_024450298.1:c.7409G= XP_024306066.1:p.Arg2470=
XM_024450299.1:c.7337G= XP_024306067.1:p.Arg2446=
XM_024450300.1:c.7199G= XP_024306068.1:p.Arg2400=
XM_024450301.1:c.5285G= XP_024306069.1:p.Arg1762=
NM_000296.4:c.7289G= NP_000287.4:p.Arg2430=
NM_001009944.3:c.7289G= MANE Select NP_001009944.3:p.Arg2430=