Canonical Allele Identifier: CA394376450
Gene: PKD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2109631T>G , CM000678.2:g.2109631T>G GRCh38
NC_000016.9:g.2159632T>G , CM000678.1:g.2159632T>G GRCh37
NC_000016.8:g.2099633T>G NCBI36
NG_008617.1:g.31268A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.5536A>C MANE Select ENSP00000262304.4:p.Ser1846Arg
ENST00000262304.8:c.5536A>C ENSP00000262304.4:p.Ser1846Arg
ENST00000415938.7:n.311-2683A>C
ENST00000423118.5:c.5536A>C ENSP00000399501.1:p.Ser1846Arg
ENST00000468674.5:n.431-281A>C
ENST00000483024.1:c.233+2185A>C
ENST00000483731.5:n.791-2683A>C
ENST00000487932.5:c.223A>C ENSP00000457132.1:p.Ser75Arg
ENST00000488185.2:c.473-1273A>C
ENST00000565639.6:n.774-2683A>C
ENST00000568591.5:c.2227-2683A>C ENSP00000457162.1:n.2227-2683A>C
ENST00000569983.5:n.422-2683A>C
NM_000296.3:c.5536A>C NP_000287.3:p.Ser1846Arg
NM_001009944.2:c.5536A>C NP_001009944.2:p.Ser1846Arg
XM_005255370.2:c.2491A>C XP_005255427.1:p.Ser831Arg
XM_011522525.1:c.5614A>C XP_011520827.1:p.Ser1872Arg
XM_011522526.1:c.5614A>C XP_011520828.1:p.Ser1872Arg
XM_011522527.1:c.5614A>C XP_011520829.1:p.Ser1872Arg
XM_011522528.1:c.5590A>C XP_011520830.1:p.Ser1864Arg
XM_011522529.1:c.5590A>C XP_011520831.1:p.Ser1864Arg
XM_011522530.1:c.5560A>C XP_011520832.1:p.Ser1854Arg
XM_011522531.1:c.5542A>C XP_011520833.1:p.Ser1848Arg
XM_011522532.1:c.5488A>C XP_011520834.1:p.Ser1830Arg
XM_011522533.1:c.5407A>C XP_011520835.1:p.Ser1803Arg
XM_011522534.1:c.5350A>C XP_011520836.1:p.Ser1784Arg
XM_011522535.1:c.3436A>C XP_011520837.1:p.Ser1146Arg
XM_011522536.1:c.5614A>C XP_011520838.1:p.Ser1872Arg
XM_011522537.1:c.2614A>C XP_011520839.1:p.Ser872Arg
XR_932867.1:n.5629A>C
XR_932868.1:n.5629A>C
XR_932869.1:n.5629A>C
XR_932870.1:n.5629A>C
XM_005255370.3:c.2491A>C XP_005255427.1:p.Ser831Arg
XM_011522528.3:c.5590A>C XP_011520830.1:p.Ser1864Arg
XM_011522529.2:c.5590A>C XP_011520831.1:p.Ser1864Arg
XM_011522537.2:c.2614A>C XP_011520839.1:p.Ser872Arg
XM_024450298.1:c.5656A>C XP_024306066.1:p.Ser1886Arg
XM_024450299.1:c.5584A>C XP_024306067.1:p.Ser1862Arg
XM_024450300.1:c.5446A>C XP_024306068.1:p.Ser1816Arg
XM_024450301.1:c.3532A>C XP_024306069.1:p.Ser1178Arg
NM_000296.4:c.5536A>C NP_000287.4:p.Ser1846Arg
NM_001009944.3:c.5536A>C MANE Select NP_001009944.3:p.Ser1846Arg