Canonical Allele Identifier: CA2202047791
Gene: PKD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2111720G= , CM000678.2:g.2111720G= GRCh38
NC_000016.9:g.2161721G= , CM000678.1:g.2161721G= GRCh37
NC_000016.8:g.2101722G= NCBI36
NG_008617.1:g.29179C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.3447C= MANE Select ENSP00000262304.4:p.His1149=
ENST00000262304.8:c.3447C= ENSP00000262304.4:p.His1149=
ENST00000415938.7:n.310+620C=
ENST00000423118.5:c.3447C= ENSP00000399501.1:p.His1149=
ENST00000468674.5:n.430+620C=
ENST00000469241.2:n.397C=
ENST00000483024.1:c.233+96C=
ENST00000483731.5:n.790+620C=
ENST00000488185.2:c.473-3362C=
ENST00000565639.6:n.773+620C=
ENST00000568591.5:c.2226+620C= ENSP00000457162.1:n.2226+620C=
ENST00000569983.5:n.421+620C=
NM_000296.3:c.3447C= NP_000287.3:p.His1149=
NM_001009944.2:c.3447C= NP_001009944.2:p.His1149=
XM_005255370.2:c.402C= XP_005255427.1:p.His134=
XM_011522525.1:c.3525C= XP_011520827.1:p.His1175=
XM_011522526.1:c.3525C= XP_011520828.1:p.His1175=
XM_011522527.1:c.3525C= XP_011520829.1:p.His1175=
XM_011522528.1:c.3501C= XP_011520830.1:p.His1167=
XM_011522529.1:c.3501C= XP_011520831.1:p.His1167=
XM_011522530.1:c.3471C= XP_011520832.1:p.His1157=
XM_011522531.1:c.3453C= XP_011520833.1:p.His1151=
XM_011522532.1:c.3399C= XP_011520834.1:p.His1133=
XM_011522533.1:c.3318C= XP_011520835.1:p.His1106=
XM_011522534.1:c.3261C= XP_011520836.1:p.His1087=
XM_011522535.1:c.1347C= XP_011520837.1:p.His449=
XM_011522536.1:c.3525C= XP_011520838.1:p.His1175=
XM_011522537.1:c.525C= XP_011520839.1:p.His175=
XR_932867.1:n.3540C=
XR_932868.1:n.3540C=
XR_932869.1:n.3540C=
XR_932870.1:n.3540C=
XM_005255370.3:c.402C= XP_005255427.1:p.His134=
XM_011522528.3:c.3501C= XP_011520830.1:p.His1167=
XM_011522529.2:c.3501C= XP_011520831.1:p.His1167=
XM_011522537.2:c.525C= XP_011520839.1:p.His175=
XM_024450298.1:c.3567C= XP_024306066.1:p.His1189=
XM_024450299.1:c.3495C= XP_024306067.1:p.His1165=
XM_024450300.1:c.3357C= XP_024306068.1:p.His1119=
XM_024450301.1:c.1443C= XP_024306069.1:p.His481=
NM_000296.4:c.3447C= NP_000287.4:p.His1149=
NM_001009944.3:c.3447C= MANE Select NP_001009944.3:p.His1149=