Canonical Allele Identifier: CA620705680
Gene: PKD1 HGNC NCBI
MIR6511B1 HGNC NCBI

Linked Data

dbSNP Id: rs2092348214
MyVariant Identifiers: chr16:g.2156689del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2106689del , CM000678.2:g.2106689del GRCh38
NC_000016.9:g.2156690del , CM000678.1:g.2156690del GRCh37
NC_000016.8:g.2096691del NCBI36
NG_008617.1:g.34211del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.7210-11del (PKD1) MANE Select ENSP00000262304.4:n.7210-11del
ENST00000262304.8:c.7210-11del (PKD1) ENSP00000262304.4:n.7210-11del
ENST00000415938.7:n.455-11del (PKD1)
ENST00000423118.5:c.7210-11del (PKD1) ENSP00000399501.1:n.7210-11del
ENST00000483024.1:c.378-11del (PKD1)
ENST00000483558.5:n.269-11del (PKD1)
ENST00000483731.5:n.935-11del (PKD1)
ENST00000486339.6:n.956-11del (PKD1)
ENST00000487932.5:c.1897-11del (PKD1) ENSP00000457132.1:n.1897-11del
ENST00000496574.6:n.1213-11del (PKD1)
ENST00000565639.6:n.918-11del (PKD1)
ENST00000568591.5:c.2371-11del (PKD1) ENSP00000457162.1:n.2371-11del
ENST00000569983.5:n.566-11del (PKD1)
NM_000296.3:c.7210-11del (PKD1) NP_000287.3:n.7210-11del
NM_001009944.2:c.7210-11del (PKD1) NP_001009944.2:n.7210-11del
NR_106775.1:n.66del (MIR6511B1)
XM_005255370.2:c.4165-11del (PKD1) XP_005255427.1:n.4165-11del
XM_011522525.1:c.7288-11del (PKD1) XP_011520827.1:n.7288-11del
XM_011522526.1:c.7288-11del (PKD1) XP_011520828.1:n.7288-11del
XM_011522527.1:c.7288-11del (PKD1) XP_011520829.1:n.7288-11del
XM_011522528.1:c.7264-11del (PKD1) XP_011520830.1:n.7264-11del
XM_011522529.1:c.7264-11del (PKD1) XP_011520831.1:n.7264-11del
XM_011522530.1:c.7234-11del (PKD1) XP_011520832.1:n.7234-11del
XM_011522531.1:c.7216-11del (PKD1) XP_011520833.1:n.7216-11del
XM_011522532.1:c.7162-11del (PKD1) XP_011520834.1:n.7162-11del
XM_011522533.1:c.7081-11del (PKD1) XP_011520835.1:n.7081-11del
XM_011522534.1:c.7024-11del (PKD1) XP_011520836.1:n.7024-11del
XM_011522535.1:c.5110-11del (PKD1) XP_011520837.1:n.5110-11del
XM_011522536.1:c.7288-11del (PKD1) XP_011520838.1:n.7288-11del
XM_011522537.1:c.4288-11del (PKD1) XP_011520839.1:n.4288-11del
XR_932867.1:n.7303-11del (PKD1)
XR_932868.1:n.7303-11del (PKD1)
XR_932869.1:n.7303-11del (PKD1)
XR_932870.1:n.7303-11del (PKD1)
XM_005255370.3:c.4165-11del (PKD1) XP_005255427.1:n.4165-11del
XM_011522528.3:c.7264-11del (PKD1) XP_011520830.1:n.7264-11del
XM_011522529.2:c.7264-11del (PKD1) XP_011520831.1:n.7264-11del
XM_011522537.2:c.4288-11del (PKD1) XP_011520839.1:n.4288-11del
XM_024450298.1:c.7330-11del (PKD1) XP_024306066.1:n.7330-11del
XM_024450299.1:c.7258-11del (PKD1) XP_024306067.1:n.7258-11del
XM_024450300.1:c.7120-11del (PKD1) XP_024306068.1:n.7120-11del
XM_024450301.1:c.5206-11del (PKD1) XP_024306069.1:n.5206-11del
NM_000296.4:c.7210-11del (PKD1) NP_000287.4:n.7210-11del
NM_001009944.3:c.7210-11del (PKD1) MANE Select NP_001009944.3:n.7210-11del