Canonical Allele Identifier: CA2202035337
Gene: PKD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2106611T= , CM000678.2:g.2106611T= GRCh38
NC_000016.9:g.2156612T= , CM000678.1:g.2156612T= GRCh37
NC_000016.8:g.2096613T= NCBI36
NG_008617.1:g.34288A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.7276A= MANE Select ENSP00000262304.4:p.Ser2426=
ENST00000262304.8:c.7276A= ENSP00000262304.4:p.Ser2426=
ENST00000415938.7:n.521A=
ENST00000423118.5:c.7276A= ENSP00000399501.1:p.Ser2426=
ENST00000483024.1:c.444A=
ENST00000483558.5:n.335A=
ENST00000483731.5:n.1001A=
ENST00000486339.6:n.1022A=
ENST00000487932.5:c.1963A= ENSP00000457132.1:p.Ser655=
ENST00000496574.6:n.1279A=
ENST00000565639.6:n.984A=
ENST00000568591.5:c.2437A= ENSP00000457162.1:n.2437A=
ENST00000569983.5:n.632A=
NM_000296.3:c.7276A= NP_000287.3:p.Ser2426=
NM_001009944.2:c.7276A= NP_001009944.2:p.Ser2426=
XM_005255370.2:c.4231A= XP_005255427.1:p.Ser1411=
XM_011522525.1:c.7354A= XP_011520827.1:p.Ser2452=
XM_011522526.1:c.7354A= XP_011520828.1:p.Ser2452=
XM_011522527.1:c.7354A= XP_011520829.1:p.Ser2452=
XM_011522528.1:c.7330A= XP_011520830.1:p.Ser2444=
XM_011522529.1:c.7330A= XP_011520831.1:p.Ser2444=
XM_011522530.1:c.7300A= XP_011520832.1:p.Ser2434=
XM_011522531.1:c.7282A= XP_011520833.1:p.Ser2428=
XM_011522532.1:c.7228A= XP_011520834.1:p.Ser2410=
XM_011522533.1:c.7147A= XP_011520835.1:p.Ser2383=
XM_011522534.1:c.7090A= XP_011520836.1:p.Ser2364=
XM_011522535.1:c.5176A= XP_011520837.1:p.Ser1726=
XM_011522536.1:c.7354A= XP_011520838.1:p.Ser2452=
XM_011522537.1:c.4354A= XP_011520839.1:p.Ser1452=
XR_932867.1:n.7369A=
XR_932868.1:n.7369A=
XR_932869.1:n.7369A=
XR_932870.1:n.7369A=
XM_005255370.3:c.4231A= XP_005255427.1:p.Ser1411=
XM_011522528.3:c.7330A= XP_011520830.1:p.Ser2444=
XM_011522529.2:c.7330A= XP_011520831.1:p.Ser2444=
XM_011522537.2:c.4354A= XP_011520839.1:p.Ser1452=
XM_024450298.1:c.7396A= XP_024306066.1:p.Ser2466=
XM_024450299.1:c.7324A= XP_024306067.1:p.Ser2442=
XM_024450300.1:c.7186A= XP_024306068.1:p.Ser2396=
XM_024450301.1:c.5272A= XP_024306069.1:p.Ser1758=
NM_000296.4:c.7276A= NP_000287.4:p.Ser2426=
NM_001009944.3:c.7276A= MANE Select NP_001009944.3:p.Ser2426=