Canonical Allele Identifier: CA394393081
Gene: PKD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2117838A>T , CM000678.2:g.2117838A>T GRCh38
NC_000016.9:g.2167839A>T , CM000678.1:g.2167839A>T GRCh37
NC_000016.8:g.2107840A>T NCBI36
NG_008617.1:g.23061T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.1154T>A MANE Select ENSP00000262304.4:p.Leu385Gln
ENST00000262304.8:c.1154T>A ENSP00000262304.4:p.Leu385Gln
ENST00000423118.5:c.1154T>A ENSP00000399501.1:p.Leu385Gln
ENST00000488185.2:c.241T>A
ENST00000568591.5:c.122T>A ENSP00000457162.1:p.Leu41Gln
ENST00000570150.1:n.287T>A
NM_000296.3:c.1154T>A NP_000287.3:p.Leu385Gln
NM_001009944.2:c.1154T>A NP_001009944.2:p.Leu385Gln
XM_011522525.1:c.1208T>A XP_011520827.1:p.Leu403Gln
XM_011522526.1:c.1208T>A XP_011520828.1:p.Leu403Gln
XM_011522527.1:c.1208T>A XP_011520829.1:p.Leu403Gln
XM_011522528.1:c.1208T>A XP_011520830.1:p.Leu403Gln
XM_011522529.1:c.1208T>A XP_011520831.1:p.Leu403Gln
XM_011522530.1:c.1154T>A XP_011520832.1:p.Leu385Gln
XM_011522531.1:c.1136T>A XP_011520833.1:p.Leu379Gln
XM_011522532.1:c.1082T>A XP_011520834.1:p.Leu361Gln
XM_011522533.1:c.1001T>A XP_011520835.1:p.Leu334Gln
XM_011522534.1:c.944T>A XP_011520836.1:p.Leu315Gln
XM_011522536.1:c.1208T>A XP_011520838.1:p.Leu403Gln
XR_932867.1:n.1223T>A
XR_932868.1:n.1223T>A
XR_932869.1:n.1223T>A
XR_932870.1:n.1223T>A
XM_011522528.3:c.1208T>A XP_011520830.1:p.Leu403Gln
XM_011522529.2:c.1208T>A XP_011520831.1:p.Leu403Gln
XM_024450298.1:c.1154T>A XP_024306066.1:p.Leu385Gln
XM_024450299.1:c.1082T>A XP_024306067.1:p.Leu361Gln
XM_024450300.1:c.944T>A XP_024306068.1:p.Leu315Gln
NM_000296.4:c.1154T>A NP_000287.4:p.Leu385Gln
NM_001009944.3:c.1154T>A MANE Select NP_001009944.3:p.Leu385Gln