Canonical Allele Identifier: CA2202047771
Gene: PKD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2111689T= , CM000678.2:g.2111689T= GRCh38
NC_000016.9:g.2161690T= , CM000678.1:g.2161690T= GRCh37
NC_000016.8:g.2101691T= NCBI36
NG_008617.1:g.29210A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.3478A= MANE Select ENSP00000262304.4:p.Thr1160=
ENST00000262304.8:c.3478A= ENSP00000262304.4:p.Thr1160=
ENST00000415938.7:n.310+651A=
ENST00000423118.5:c.3478A= ENSP00000399501.1:p.Thr1160=
ENST00000468674.5:n.430+651A=
ENST00000469241.2:n.428A=
ENST00000483024.1:c.233+127A=
ENST00000483731.5:n.790+651A=
ENST00000488185.2:c.473-3331A=
ENST00000565639.6:n.773+651A=
ENST00000568591.5:c.2226+651A= ENSP00000457162.1:n.2226+651A=
ENST00000569983.5:n.421+651A=
NM_000296.3:c.3478A= NP_000287.3:p.Thr1160=
NM_001009944.2:c.3478A= NP_001009944.2:p.Thr1160=
XM_005255370.2:c.433A= XP_005255427.1:p.Thr145=
XM_011522525.1:c.3556A= XP_011520827.1:p.Thr1186=
XM_011522526.1:c.3556A= XP_011520828.1:p.Thr1186=
XM_011522527.1:c.3556A= XP_011520829.1:p.Thr1186=
XM_011522528.1:c.3532A= XP_011520830.1:p.Thr1178=
XM_011522529.1:c.3532A= XP_011520831.1:p.Thr1178=
XM_011522530.1:c.3502A= XP_011520832.1:p.Thr1168=
XM_011522531.1:c.3484A= XP_011520833.1:p.Thr1162=
XM_011522532.1:c.3430A= XP_011520834.1:p.Thr1144=
XM_011522533.1:c.3349A= XP_011520835.1:p.Thr1117=
XM_011522534.1:c.3292A= XP_011520836.1:p.Thr1098=
XM_011522535.1:c.1378A= XP_011520837.1:p.Thr460=
XM_011522536.1:c.3556A= XP_011520838.1:p.Thr1186=
XM_011522537.1:c.556A= XP_011520839.1:p.Thr186=
XR_932867.1:n.3571A=
XR_932868.1:n.3571A=
XR_932869.1:n.3571A=
XR_932870.1:n.3571A=
XM_005255370.3:c.433A= XP_005255427.1:p.Thr145=
XM_011522528.3:c.3532A= XP_011520830.1:p.Thr1178=
XM_011522529.2:c.3532A= XP_011520831.1:p.Thr1178=
XM_011522537.2:c.556A= XP_011520839.1:p.Thr186=
XM_024450298.1:c.3598A= XP_024306066.1:p.Thr1200=
XM_024450299.1:c.3526A= XP_024306067.1:p.Thr1176=
XM_024450300.1:c.3388A= XP_024306068.1:p.Thr1130=
XM_024450301.1:c.1474A= XP_024306069.1:p.Thr492=
NM_000296.4:c.3478A= NP_000287.4:p.Thr1160=
NM_001009944.3:c.3478A= MANE Select NP_001009944.3:p.Thr1160=