Canonical Allele Identifier: CA2202035469
Gene: PKD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2106632C= , CM000678.2:g.2106632C= GRCh38
NC_000016.9:g.2156633C= , CM000678.1:g.2156633C= GRCh37
NC_000016.8:g.2096634C= NCBI36
NG_008617.1:g.34267G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.7255G= MANE Select ENSP00000262304.4:p.Glu2419=
ENST00000262304.8:c.7255G= ENSP00000262304.4:p.Glu2419=
ENST00000415938.7:n.500G=
ENST00000423118.5:c.7255G= ENSP00000399501.1:p.Glu2419=
ENST00000483024.1:c.423G=
ENST00000483558.5:n.314G=
ENST00000483731.5:n.980G=
ENST00000486339.6:n.1001G=
ENST00000487932.5:c.1942G= ENSP00000457132.1:p.Glu648=
ENST00000496574.6:n.1258G=
ENST00000565639.6:n.963G=
ENST00000568591.5:c.2416G= ENSP00000457162.1:n.2416G=
ENST00000569983.5:n.611G=
NM_000296.3:c.7255G= NP_000287.3:p.Glu2419=
NM_001009944.2:c.7255G= NP_001009944.2:p.Glu2419=
XM_005255370.2:c.4210G= XP_005255427.1:p.Glu1404=
XM_011522525.1:c.7333G= XP_011520827.1:p.Glu2445=
XM_011522526.1:c.7333G= XP_011520828.1:p.Glu2445=
XM_011522527.1:c.7333G= XP_011520829.1:p.Glu2445=
XM_011522528.1:c.7309G= XP_011520830.1:p.Glu2437=
XM_011522529.1:c.7309G= XP_011520831.1:p.Glu2437=
XM_011522530.1:c.7279G= XP_011520832.1:p.Glu2427=
XM_011522531.1:c.7261G= XP_011520833.1:p.Glu2421=
XM_011522532.1:c.7207G= XP_011520834.1:p.Glu2403=
XM_011522533.1:c.7126G= XP_011520835.1:p.Glu2376=
XM_011522534.1:c.7069G= XP_011520836.1:p.Glu2357=
XM_011522535.1:c.5155G= XP_011520837.1:p.Glu1719=
XM_011522536.1:c.7333G= XP_011520838.1:p.Glu2445=
XM_011522537.1:c.4333G= XP_011520839.1:p.Glu1445=
XR_932867.1:n.7348G=
XR_932868.1:n.7348G=
XR_932869.1:n.7348G=
XR_932870.1:n.7348G=
XM_005255370.3:c.4210G= XP_005255427.1:p.Glu1404=
XM_011522528.3:c.7309G= XP_011520830.1:p.Glu2437=
XM_011522529.2:c.7309G= XP_011520831.1:p.Glu2437=
XM_011522537.2:c.4333G= XP_011520839.1:p.Glu1445=
XM_024450298.1:c.7375G= XP_024306066.1:p.Glu2459=
XM_024450299.1:c.7303G= XP_024306067.1:p.Glu2435=
XM_024450300.1:c.7165G= XP_024306068.1:p.Glu2389=
XM_024450301.1:c.5251G= XP_024306069.1:p.Glu1751=
NM_000296.4:c.7255G= NP_000287.4:p.Glu2419=
NM_001009944.3:c.7255G= MANE Select NP_001009944.3:p.Glu2419=