Canonical Allele Identifier: CA2202034770
Gene: PKD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2106515C= , CM000678.2:g.2106515C= GRCh38
NC_000016.9:g.2156516C= , CM000678.1:g.2156516C= GRCh37
NC_000016.8:g.2096517C= NCBI36
NG_008617.1:g.34384G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.7372G= MANE Select ENSP00000262304.4:p.Glu2458=
ENST00000262304.8:c.7372G= ENSP00000262304.4:p.Glu2458=
ENST00000415938.7:n.617G=
ENST00000423118.5:c.7372G= ENSP00000399501.1:p.Glu2458=
ENST00000483558.5:n.431G=
ENST00000483731.5:n.1097G=
ENST00000486339.6:n.1118G=
ENST00000487932.5:c.2059G= ENSP00000457132.1:p.Glu687=
ENST00000496574.6:n.1375G=
ENST00000565639.6:n.1080G=
ENST00000568591.5:c.2533G= ENSP00000457162.1:n.2533G=
NM_000296.3:c.7372G= NP_000287.3:p.Glu2458=
NM_001009944.2:c.7372G= NP_001009944.2:p.Glu2458=
XM_005255370.2:c.4327G= XP_005255427.1:p.Glu1443=
XM_011522525.1:c.7450G= XP_011520827.1:p.Glu2484=
XM_011522526.1:c.7450G= XP_011520828.1:p.Glu2484=
XM_011522527.1:c.7450G= XP_011520829.1:p.Glu2484=
XM_011522528.1:c.7426G= XP_011520830.1:p.Glu2476=
XM_011522529.1:c.7426G= XP_011520831.1:p.Glu2476=
XM_011522530.1:c.7396G= XP_011520832.1:p.Glu2466=
XM_011522531.1:c.7378G= XP_011520833.1:p.Glu2460=
XM_011522532.1:c.7324G= XP_011520834.1:p.Glu2442=
XM_011522533.1:c.7243G= XP_011520835.1:p.Glu2415=
XM_011522534.1:c.7186G= XP_011520836.1:p.Glu2396=
XM_011522535.1:c.5272G= XP_011520837.1:p.Glu1758=
XM_011522536.1:c.7450G= XP_011520838.1:p.Glu2484=
XM_011522537.1:c.4450G= XP_011520839.1:p.Glu1484=
XR_932867.1:n.7465G=
XR_932868.1:n.7465G=
XR_932869.1:n.7465G=
XR_932870.1:n.7465G=
XM_005255370.3:c.4327G= XP_005255427.1:p.Glu1443=
XM_011522528.3:c.7426G= XP_011520830.1:p.Glu2476=
XM_011522529.2:c.7426G= XP_011520831.1:p.Glu2476=
XM_011522537.2:c.4450G= XP_011520839.1:p.Glu1484=
XM_024450298.1:c.7492G= XP_024306066.1:p.Glu2498=
XM_024450299.1:c.7420G= XP_024306067.1:p.Glu2474=
XM_024450300.1:c.7282G= XP_024306068.1:p.Glu2428=
XM_024450301.1:c.5368G= XP_024306069.1:p.Glu1790=
NM_000296.4:c.7372G= NP_000287.4:p.Glu2458=
NM_001009944.3:c.7372G= MANE Select NP_001009944.3:p.Glu2458=