Canonical Allele Identifier: CA2202034872
Gene: PKD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2106536G= , CM000678.2:g.2106536G= GRCh38
NC_000016.9:g.2156537G= , CM000678.1:g.2156537G= GRCh37
NC_000016.8:g.2096538G= NCBI36
NG_008617.1:g.34363C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.7351C= MANE Select ENSP00000262304.4:p.Leu2451=
ENST00000262304.8:c.7351C= ENSP00000262304.4:p.Leu2451=
ENST00000415938.7:n.596C=
ENST00000423118.5:c.7351C= ENSP00000399501.1:p.Leu2451=
ENST00000483558.5:n.410C=
ENST00000483731.5:n.1076C=
ENST00000486339.6:n.1097C=
ENST00000487932.5:c.2038C= ENSP00000457132.1:p.Leu680=
ENST00000496574.6:n.1354C=
ENST00000565639.6:n.1059C=
ENST00000568591.5:c.2512C= ENSP00000457162.1:n.2512C=
ENST00000569983.5:n.707C=
NM_000296.3:c.7351C= NP_000287.3:p.Leu2451=
NM_001009944.2:c.7351C= NP_001009944.2:p.Leu2451=
XM_005255370.2:c.4306C= XP_005255427.1:p.Leu1436=
XM_011522525.1:c.7429C= XP_011520827.1:p.Leu2477=
XM_011522526.1:c.7429C= XP_011520828.1:p.Leu2477=
XM_011522527.1:c.7429C= XP_011520829.1:p.Leu2477=
XM_011522528.1:c.7405C= XP_011520830.1:p.Leu2469=
XM_011522529.1:c.7405C= XP_011520831.1:p.Leu2469=
XM_011522530.1:c.7375C= XP_011520832.1:p.Leu2459=
XM_011522531.1:c.7357C= XP_011520833.1:p.Leu2453=
XM_011522532.1:c.7303C= XP_011520834.1:p.Leu2435=
XM_011522533.1:c.7222C= XP_011520835.1:p.Leu2408=
XM_011522534.1:c.7165C= XP_011520836.1:p.Leu2389=
XM_011522535.1:c.5251C= XP_011520837.1:p.Leu1751=
XM_011522536.1:c.7429C= XP_011520838.1:p.Leu2477=
XM_011522537.1:c.4429C= XP_011520839.1:p.Leu1477=
XR_932867.1:n.7444C=
XR_932868.1:n.7444C=
XR_932869.1:n.7444C=
XR_932870.1:n.7444C=
XM_005255370.3:c.4306C= XP_005255427.1:p.Leu1436=
XM_011522528.3:c.7405C= XP_011520830.1:p.Leu2469=
XM_011522529.2:c.7405C= XP_011520831.1:p.Leu2469=
XM_011522537.2:c.4429C= XP_011520839.1:p.Leu1477=
XM_024450298.1:c.7471C= XP_024306066.1:p.Leu2491=
XM_024450299.1:c.7399C= XP_024306067.1:p.Leu2467=
XM_024450300.1:c.7261C= XP_024306068.1:p.Leu2421=
XM_024450301.1:c.5347C= XP_024306069.1:p.Leu1783=
NM_000296.4:c.7351C= NP_000287.4:p.Leu2451=
NM_001009944.3:c.7351C= MANE Select NP_001009944.3:p.Leu2451=