Canonical Allele Identifier: CA394393466
Gene: PKD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2117922G>C , CM000678.2:g.2117922G>C GRCh38
NC_000016.9:g.2167923G>C , CM000678.1:g.2167923G>C GRCh37
NC_000016.8:g.2107924G>C NCBI36
NG_008617.1:g.22977C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262304.9:c.1070C>G MANE Select ENSP00000262304.4:p.Ala357Gly
ENST00000262304.8:c.1070C>G ENSP00000262304.4:p.Ala357Gly
ENST00000423118.5:c.1070C>G ENSP00000399501.1:p.Ala357Gly
ENST00000488185.2:c.157C>G
ENST00000568591.5:c.38C>G ENSP00000457162.1:p.Ala13Gly
ENST00000570150.1:n.203C>G
NM_000296.3:c.1070C>G NP_000287.3:p.Ala357Gly
NM_001009944.2:c.1070C>G NP_001009944.2:p.Ala357Gly
XM_011522525.1:c.1124C>G XP_011520827.1:p.Ala375Gly
XM_011522526.1:c.1124C>G XP_011520828.1:p.Ala375Gly
XM_011522527.1:c.1124C>G XP_011520829.1:p.Ala375Gly
XM_011522528.1:c.1124C>G XP_011520830.1:p.Ala375Gly
XM_011522529.1:c.1124C>G XP_011520831.1:p.Ala375Gly
XM_011522530.1:c.1070C>G XP_011520832.1:p.Ala357Gly
XM_011522531.1:c.1052C>G XP_011520833.1:p.Ala351Gly
XM_011522532.1:c.998C>G XP_011520834.1:p.Ala333Gly
XM_011522533.1:c.917C>G XP_011520835.1:p.Ala306Gly
XM_011522534.1:c.860C>G XP_011520836.1:p.Ala287Gly
XM_011522536.1:c.1124C>G XP_011520838.1:p.Ala375Gly
XR_932867.1:n.1139C>G
XR_932868.1:n.1139C>G
XR_932869.1:n.1139C>G
XR_932870.1:n.1139C>G
XM_011522528.3:c.1124C>G XP_011520830.1:p.Ala375Gly
XM_011522529.2:c.1124C>G XP_011520831.1:p.Ala375Gly
XM_024450298.1:c.1070C>G XP_024306066.1:p.Ala357Gly
XM_024450299.1:c.998C>G XP_024306067.1:p.Ala333Gly
XM_024450300.1:c.860C>G XP_024306068.1:p.Ala287Gly
NM_000296.4:c.1070C>G NP_000287.4:p.Ala357Gly
NM_001009944.3:c.1070C>G MANE Select NP_001009944.3:p.Ala357Gly