Canonical Allele Identifier: CA2202047758
Gene: PKD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2111673T= , CM000678.2:g.2111673T= GRCh38
NC_000016.9:g.2161674T= , CM000678.1:g.2161674T= GRCh37
NC_000016.8:g.2101675T= NCBI36
NG_008617.1:g.29226A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.3494A= MANE Select ENSP00000262304.4:p.Asp1165=
ENST00000262304.8:c.3494A= ENSP00000262304.4:p.Asp1165=
ENST00000415938.7:n.310+667A=
ENST00000423118.5:c.3494A= ENSP00000399501.1:p.Asp1165=
ENST00000468674.5:n.430+667A=
ENST00000469241.2:n.444A=
ENST00000483024.1:c.233+143A=
ENST00000483731.5:n.790+667A=
ENST00000488185.2:c.473-3315A=
ENST00000565639.6:n.773+667A=
ENST00000568591.5:c.2226+667A= ENSP00000457162.1:n.2226+667A=
ENST00000569983.5:n.421+667A=
NM_000296.3:c.3494A= NP_000287.3:p.Asp1165=
NM_001009944.2:c.3494A= NP_001009944.2:p.Asp1165=
XM_005255370.2:c.449A= XP_005255427.1:p.Asp150=
XM_011522525.1:c.3572A= XP_011520827.1:p.Asp1191=
XM_011522526.1:c.3572A= XP_011520828.1:p.Asp1191=
XM_011522527.1:c.3572A= XP_011520829.1:p.Asp1191=
XM_011522528.1:c.3548A= XP_011520830.1:p.Asp1183=
XM_011522529.1:c.3548A= XP_011520831.1:p.Asp1183=
XM_011522530.1:c.3518A= XP_011520832.1:p.Asp1173=
XM_011522531.1:c.3500A= XP_011520833.1:p.Asp1167=
XM_011522532.1:c.3446A= XP_011520834.1:p.Asp1149=
XM_011522533.1:c.3365A= XP_011520835.1:p.Asp1122=
XM_011522534.1:c.3308A= XP_011520836.1:p.Asp1103=
XM_011522535.1:c.1394A= XP_011520837.1:p.Asp465=
XM_011522536.1:c.3572A= XP_011520838.1:p.Asp1191=
XM_011522537.1:c.572A= XP_011520839.1:p.Asp191=
XR_932867.1:n.3587A=
XR_932868.1:n.3587A=
XR_932869.1:n.3587A=
XR_932870.1:n.3587A=
XM_005255370.3:c.449A= XP_005255427.1:p.Asp150=
XM_011522528.3:c.3548A= XP_011520830.1:p.Asp1183=
XM_011522529.2:c.3548A= XP_011520831.1:p.Asp1183=
XM_011522537.2:c.572A= XP_011520839.1:p.Asp191=
XM_024450298.1:c.3614A= XP_024306066.1:p.Asp1205=
XM_024450299.1:c.3542A= XP_024306067.1:p.Asp1181=
XM_024450300.1:c.3404A= XP_024306068.1:p.Asp1135=
XM_024450301.1:c.1490A= XP_024306069.1:p.Asp497=
NM_000296.4:c.3494A= NP_000287.4:p.Asp1165=
NM_001009944.3:c.3494A= MANE Select NP_001009944.3:p.Asp1165=