Canonical Allele Identifier: CA2202035490
Gene: PKD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2106638G= , CM000678.2:g.2106638G= GRCh38
NC_000016.9:g.2156639G= , CM000678.1:g.2156639G= GRCh37
NC_000016.8:g.2096640G= NCBI36
NG_008617.1:g.34261C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.7249C= MANE Select ENSP00000262304.4:p.Leu2417=
ENST00000262304.8:c.7249C= ENSP00000262304.4:p.Leu2417=
ENST00000415938.7:n.494C=
ENST00000423118.5:c.7249C= ENSP00000399501.1:p.Leu2417=
ENST00000483024.1:c.417C=
ENST00000483558.5:n.308C=
ENST00000483731.5:n.974C=
ENST00000486339.6:n.995C=
ENST00000487932.5:c.1936C= ENSP00000457132.1:p.Leu646=
ENST00000496574.6:n.1252C=
ENST00000565639.6:n.957C=
ENST00000568591.5:c.2410C= ENSP00000457162.1:n.2410C=
ENST00000569983.5:n.605C=
NM_000296.3:c.7249C= NP_000287.3:p.Leu2417=
NM_001009944.2:c.7249C= NP_001009944.2:p.Leu2417=
XM_005255370.2:c.4204C= XP_005255427.1:p.Leu1402=
XM_011522525.1:c.7327C= XP_011520827.1:p.Leu2443=
XM_011522526.1:c.7327C= XP_011520828.1:p.Leu2443=
XM_011522527.1:c.7327C= XP_011520829.1:p.Leu2443=
XM_011522528.1:c.7303C= XP_011520830.1:p.Leu2435=
XM_011522529.1:c.7303C= XP_011520831.1:p.Leu2435=
XM_011522530.1:c.7273C= XP_011520832.1:p.Leu2425=
XM_011522531.1:c.7255C= XP_011520833.1:p.Leu2419=
XM_011522532.1:c.7201C= XP_011520834.1:p.Leu2401=
XM_011522533.1:c.7120C= XP_011520835.1:p.Leu2374=
XM_011522534.1:c.7063C= XP_011520836.1:p.Leu2355=
XM_011522535.1:c.5149C= XP_011520837.1:p.Leu1717=
XM_011522536.1:c.7327C= XP_011520838.1:p.Leu2443=
XM_011522537.1:c.4327C= XP_011520839.1:p.Leu1443=
XR_932867.1:n.7342C=
XR_932868.1:n.7342C=
XR_932869.1:n.7342C=
XR_932870.1:n.7342C=
XM_005255370.3:c.4204C= XP_005255427.1:p.Leu1402=
XM_011522528.3:c.7303C= XP_011520830.1:p.Leu2435=
XM_011522529.2:c.7303C= XP_011520831.1:p.Leu2435=
XM_011522537.2:c.4327C= XP_011520839.1:p.Leu1443=
XM_024450298.1:c.7369C= XP_024306066.1:p.Leu2457=
XM_024450299.1:c.7297C= XP_024306067.1:p.Leu2433=
XM_024450300.1:c.7159C= XP_024306068.1:p.Leu2387=
XM_024450301.1:c.5245C= XP_024306069.1:p.Leu1749=
NM_000296.4:c.7249C= NP_000287.4:p.Leu2417=
NM_001009944.3:c.7249C= MANE Select NP_001009944.3:p.Leu2417=