Canonical Allele Identifier: CA2202034839
Gene: PKD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2106530G= , CM000678.2:g.2106530G= GRCh38
NC_000016.9:g.2156531G= , CM000678.1:g.2156531G= GRCh37
NC_000016.8:g.2096532G= NCBI36
NG_008617.1:g.34369C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.7357C= MANE Select ENSP00000262304.4:p.Arg2453=
ENST00000262304.8:c.7357C= ENSP00000262304.4:p.Arg2453=
ENST00000415938.7:n.602C=
ENST00000423118.5:c.7357C= ENSP00000399501.1:p.Arg2453=
ENST00000483558.5:n.416C=
ENST00000483731.5:n.1082C=
ENST00000486339.6:n.1103C=
ENST00000487932.5:c.2044C= ENSP00000457132.1:p.Arg682=
ENST00000496574.6:n.1360C=
ENST00000565639.6:n.1065C=
ENST00000568591.5:c.2518C= ENSP00000457162.1:n.2518C=
ENST00000569983.5:n.713C=
NM_000296.3:c.7357C= NP_000287.3:p.Arg2453=
NM_001009944.2:c.7357C= NP_001009944.2:p.Arg2453=
XM_005255370.2:c.4312C= XP_005255427.1:p.Arg1438=
XM_011522525.1:c.7435C= XP_011520827.1:p.Arg2479=
XM_011522526.1:c.7435C= XP_011520828.1:p.Arg2479=
XM_011522527.1:c.7435C= XP_011520829.1:p.Arg2479=
XM_011522528.1:c.7411C= XP_011520830.1:p.Arg2471=
XM_011522529.1:c.7411C= XP_011520831.1:p.Arg2471=
XM_011522530.1:c.7381C= XP_011520832.1:p.Arg2461=
XM_011522531.1:c.7363C= XP_011520833.1:p.Arg2455=
XM_011522532.1:c.7309C= XP_011520834.1:p.Arg2437=
XM_011522533.1:c.7228C= XP_011520835.1:p.Arg2410=
XM_011522534.1:c.7171C= XP_011520836.1:p.Arg2391=
XM_011522535.1:c.5257C= XP_011520837.1:p.Arg1753=
XM_011522536.1:c.7435C= XP_011520838.1:p.Arg2479=
XM_011522537.1:c.4435C= XP_011520839.1:p.Arg1479=
XR_932867.1:n.7450C=
XR_932868.1:n.7450C=
XR_932869.1:n.7450C=
XR_932870.1:n.7450C=
XM_005255370.3:c.4312C= XP_005255427.1:p.Arg1438=
XM_011522528.3:c.7411C= XP_011520830.1:p.Arg2471=
XM_011522529.2:c.7411C= XP_011520831.1:p.Arg2471=
XM_011522537.2:c.4435C= XP_011520839.1:p.Arg1479=
XM_024450298.1:c.7477C= XP_024306066.1:p.Arg2493=
XM_024450299.1:c.7405C= XP_024306067.1:p.Arg2469=
XM_024450300.1:c.7267C= XP_024306068.1:p.Arg2423=
XM_024450301.1:c.5353C= XP_024306069.1:p.Arg1785=
NM_000296.4:c.7357C= NP_000287.4:p.Arg2453=
NM_001009944.3:c.7357C= MANE Select NP_001009944.3:p.Arg2453=