Canonical Allele Identifier: CA2202034913
Gene: PKD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2106549G= , CM000678.2:g.2106549G= GRCh38
NC_000016.9:g.2156550G= , CM000678.1:g.2156550G= GRCh37
NC_000016.8:g.2096551G= NCBI36
NG_008617.1:g.34350C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.7338C= MANE Select ENSP00000262304.4:p.Phe2446=
ENST00000262304.8:c.7338C= ENSP00000262304.4:p.Phe2446=
ENST00000415938.7:n.583C=
ENST00000423118.5:c.7338C= ENSP00000399501.1:p.Phe2446=
ENST00000483558.5:n.397C=
ENST00000483731.5:n.1063C=
ENST00000486339.6:n.1084C=
ENST00000487932.5:c.2025C= ENSP00000457132.1:p.Phe675=
ENST00000496574.6:n.1341C=
ENST00000565639.6:n.1046C=
ENST00000568591.5:c.2499C= ENSP00000457162.1:n.2499C=
ENST00000569983.5:n.694C=
NM_000296.3:c.7338C= NP_000287.3:p.Phe2446=
NM_001009944.2:c.7338C= NP_001009944.2:p.Phe2446=
XM_005255370.2:c.4293C= XP_005255427.1:p.Phe1431=
XM_011522525.1:c.7416C= XP_011520827.1:p.Phe2472=
XM_011522526.1:c.7416C= XP_011520828.1:p.Phe2472=
XM_011522527.1:c.7416C= XP_011520829.1:p.Phe2472=
XM_011522528.1:c.7392C= XP_011520830.1:p.Phe2464=
XM_011522529.1:c.7392C= XP_011520831.1:p.Phe2464=
XM_011522530.1:c.7362C= XP_011520832.1:p.Phe2454=
XM_011522531.1:c.7344C= XP_011520833.1:p.Phe2448=
XM_011522532.1:c.7290C= XP_011520834.1:p.Phe2430=
XM_011522533.1:c.7209C= XP_011520835.1:p.Phe2403=
XM_011522534.1:c.7152C= XP_011520836.1:p.Phe2384=
XM_011522535.1:c.5238C= XP_011520837.1:p.Phe1746=
XM_011522536.1:c.7416C= XP_011520838.1:p.Phe2472=
XM_011522537.1:c.4416C= XP_011520839.1:p.Phe1472=
XR_932867.1:n.7431C=
XR_932868.1:n.7431C=
XR_932869.1:n.7431C=
XR_932870.1:n.7431C=
XM_005255370.3:c.4293C= XP_005255427.1:p.Phe1431=
XM_011522528.3:c.7392C= XP_011520830.1:p.Phe2464=
XM_011522529.2:c.7392C= XP_011520831.1:p.Phe2464=
XM_011522537.2:c.4416C= XP_011520839.1:p.Phe1472=
XM_024450298.1:c.7458C= XP_024306066.1:p.Phe2486=
XM_024450299.1:c.7386C= XP_024306067.1:p.Phe2462=
XM_024450300.1:c.7248C= XP_024306068.1:p.Phe2416=
XM_024450301.1:c.5334C= XP_024306069.1:p.Phe1778=
NM_000296.4:c.7338C= NP_000287.4:p.Phe2446=
NM_001009944.3:c.7338C= MANE Select NP_001009944.3:p.Phe2446=