Canonical Allele Identifier: CA394387528
Gene: PKD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2114472A>G , CM000678.2:g.2114472A>G GRCh38
NC_000016.9:g.2164473A>G , CM000678.1:g.2164473A>G GRCh37
NC_000016.8:g.2104474A>G NCBI36
NG_008617.1:g.26427T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.2551T>C MANE Select ENSP00000262304.4:p.Ser851Pro
ENST00000262304.8:c.2551T>C ENSP00000262304.4:p.Ser851Pro
ENST00000423118.5:c.2551T>C ENSP00000399501.1:p.Ser851Pro
ENST00000488185.2:c.472+3017T>C
ENST00000565639.6:n.10T>C
ENST00000568591.5:c.1482T>C ENSP00000457162.1:n.1482T>C
NM_000296.3:c.2551T>C NP_000287.3:p.Ser851Pro
NM_001009944.2:c.2551T>C NP_001009944.2:p.Ser851Pro
XM_011522525.1:c.2605T>C XP_011520827.1:p.Ser869Pro
XM_011522526.1:c.2605T>C XP_011520828.1:p.Ser869Pro
XM_011522527.1:c.2605T>C XP_011520829.1:p.Ser869Pro
XM_011522528.1:c.2605T>C XP_011520830.1:p.Ser869Pro
XM_011522529.1:c.2605T>C XP_011520831.1:p.Ser869Pro
XM_011522530.1:c.2551T>C XP_011520832.1:p.Ser851Pro
XM_011522531.1:c.2533T>C XP_011520833.1:p.Ser845Pro
XM_011522532.1:c.2479T>C XP_011520834.1:p.Ser827Pro
XM_011522533.1:c.2398T>C XP_011520835.1:p.Ser800Pro
XM_011522534.1:c.2341T>C XP_011520836.1:p.Ser781Pro
XM_011522535.1:c.427T>C XP_011520837.1:p.Ser143Pro
XM_011522536.1:c.2605T>C XP_011520838.1:p.Ser869Pro
XR_932867.1:n.2620T>C
XR_932868.1:n.2620T>C
XR_932869.1:n.2620T>C
XR_932870.1:n.2620T>C
XM_005255370.3:c.-499T>C XP_005255427.1:n.-499T>C
XM_011522528.3:c.2605T>C XP_011520830.1:p.Ser869Pro
XM_011522529.2:c.2605T>C XP_011520831.1:p.Ser869Pro
XM_024450298.1:c.2551T>C XP_024306066.1:p.Ser851Pro
XM_024450299.1:c.2479T>C XP_024306067.1:p.Ser827Pro
XM_024450300.1:c.2341T>C XP_024306068.1:p.Ser781Pro
XM_024450301.1:c.427T>C XP_024306069.1:p.Ser143Pro
NM_000296.4:c.2551T>C NP_000287.4:p.Ser851Pro
NM_001009944.3:c.2551T>C MANE Select NP_001009944.3:p.Ser851Pro