Canonical Allele Identifier: CA2202023283
Gene: PKD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2103855T= , CM000678.2:g.2103855T= GRCh38
NC_000016.9:g.2153856T= , CM000678.1:g.2153856T= GRCh37
NC_000016.8:g.2093857T= NCBI36
NG_008617.1:g.39366A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.8202A= MANE Select ENSP00000262304.4:p.Pro2734=
ENST00000262304.8:c.8202A= ENSP00000262304.4:p.Pro2734=
ENST00000415938.7:n.1447A=
ENST00000423118.5:c.8202A= ENSP00000399501.1:p.Pro2734=
ENST00000483731.5:n.1927A=
ENST00000486339.6:n.2338A=
ENST00000487932.5:c.2889A= ENSP00000457132.1:p.Pro963=
ENST00000496574.6:n.2438A=
ENST00000561991.5:n.724A=
ENST00000565639.6:n.1910A=
ENST00000567946.1:c.263A=
NM_000296.3:c.8202A= NP_000287.3:p.Pro2734=
NM_001009944.2:c.8202A= NP_001009944.2:p.Pro2734=
XM_005255370.2:c.5157A= XP_005255427.1:p.Pro1719=
XM_011522525.1:c.8280A= XP_011520827.1:p.Pro2760=
XM_011522526.1:c.8280A= XP_011520828.1:p.Pro2760=
XM_011522527.1:c.8280A= XP_011520829.1:p.Pro2760=
XM_011522528.1:c.8256A= XP_011520830.1:p.Pro2752=
XM_011522529.1:c.8256A= XP_011520831.1:p.Pro2752=
XM_011522530.1:c.8226A= XP_011520832.1:p.Pro2742=
XM_011522531.1:c.8208A= XP_011520833.1:p.Pro2736=
XM_011522532.1:c.8154A= XP_011520834.1:p.Pro2718=
XM_011522533.1:c.8073A= XP_011520835.1:p.Pro2691=
XM_011522534.1:c.8016A= XP_011520836.1:p.Pro2672=
XM_011522535.1:c.6102A= XP_011520837.1:p.Pro2034=
XM_011522536.1:c.8280A= XP_011520838.1:p.Pro2760=
XM_011522537.1:c.5280A= XP_011520839.1:p.Pro1760=
XR_932867.1:n.8295A=
XR_932868.1:n.8295A=
XR_932869.1:n.8295A=
XR_932870.1:n.8295A=
XM_005255370.3:c.5157A= XP_005255427.1:p.Pro1719=
XM_011522528.3:c.8256A= XP_011520830.1:p.Pro2752=
XM_011522529.2:c.8256A= XP_011520831.1:p.Pro2752=
XM_011522537.2:c.5280A= XP_011520839.1:p.Pro1760=
XM_024450298.1:c.8322A= XP_024306066.1:p.Pro2774=
XM_024450299.1:c.8250A= XP_024306067.1:p.Pro2750=
XM_024450300.1:c.8112A= XP_024306068.1:p.Pro2704=
XM_024450301.1:c.6198A= XP_024306069.1:p.Pro2066=
NM_000296.4:c.8202A= NP_000287.4:p.Pro2734=
NM_001009944.3:c.8202A= MANE Select NP_001009944.3:p.Pro2734=