Canonical Allele Identifier: CA7833178
Gene: PKD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 997278
ClinVar RCV Id: RCV001292297
dbSNP Id: rs181738771
gnomAD v2: 16-2164497-A-G
gnomAD v3: 16-2114496-A-G
gnomAD v4: 16-2114496-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2114496A>G , CM000678.2:g.2114496A>G GRCh38
NC_000016.9:g.2164497A>G , CM000678.1:g.2164497A>G GRCh37
NC_000016.8:g.2104498A>G NCBI36
NG_008617.1:g.26403T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.2527T>C MANE Select ENSP00000262304.4:p.Ser843Pro
ENST00000262304.8:c.2527T>C ENSP00000262304.4:p.Ser843Pro
ENST00000423118.5:c.2527T>C ENSP00000399501.1:p.Ser843Pro
ENST00000488185.2:c.472+2993T>C
ENST00000568591.5:c.1458T>C ENSP00000457162.1:n.1458T>C
NM_000296.3:c.2527T>C NP_000287.3:p.Ser843Pro
NM_001009944.2:c.2527T>C NP_001009944.2:p.Ser843Pro
XM_011522525.1:c.2581T>C XP_011520827.1:p.Ser861Pro
XM_011522526.1:c.2581T>C XP_011520828.1:p.Ser861Pro
XM_011522527.1:c.2581T>C XP_011520829.1:p.Ser861Pro
XM_011522528.1:c.2581T>C XP_011520830.1:p.Ser861Pro
XM_011522529.1:c.2581T>C XP_011520831.1:p.Ser861Pro
XM_011522530.1:c.2527T>C XP_011520832.1:p.Ser843Pro
XM_011522531.1:c.2509T>C XP_011520833.1:p.Ser837Pro
XM_011522532.1:c.2455T>C XP_011520834.1:p.Ser819Pro
XM_011522533.1:c.2374T>C XP_011520835.1:p.Ser792Pro
XM_011522534.1:c.2317T>C XP_011520836.1:p.Ser773Pro
XM_011522535.1:c.403T>C XP_011520837.1:p.Ser135Pro
XM_011522536.1:c.2581T>C XP_011520838.1:p.Ser861Pro
XR_932867.1:n.2596T>C
XR_932868.1:n.2596T>C
XR_932869.1:n.2596T>C
XR_932870.1:n.2596T>C
XM_005255370.3:c.-523T>C XP_005255427.1:n.-523T>C
XM_011522528.3:c.2581T>C XP_011520830.1:p.Ser861Pro
XM_011522529.2:c.2581T>C XP_011520831.1:p.Ser861Pro
XM_024450298.1:c.2527T>C XP_024306066.1:p.Ser843Pro
XM_024450299.1:c.2455T>C XP_024306067.1:p.Ser819Pro
XM_024450300.1:c.2317T>C XP_024306068.1:p.Ser773Pro
XM_024450301.1:c.403T>C XP_024306069.1:p.Ser135Pro
NM_000296.4:c.2527T>C NP_000287.4:p.Ser843Pro
NM_001009944.3:c.2527T>C MANE Select NP_001009944.3:p.Ser843Pro