Canonical Allele Identifier: CA2202041995
Gene: PKD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2090532C= , CM000678.2:g.2090532C= GRCh38
NC_000016.9:g.2140533C= , CM000678.1:g.2140533C= GRCh37
NC_000016.8:g.2080534C= NCBI36
NG_005895.1:g.46227C= , LRG_487:g.46227C=
NG_008617.1:g.52689G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.12197G= MANE Select ENSP00000262304.4:p.Cys4066=
ENST00000262304.8:c.12197G= ENSP00000262304.4:p.Cys4066=
ENST00000423118.5:c.12194G= ENSP00000399501.1:p.Cys4065=
ENST00000472577.1:n.225G=
NM_000296.3:c.12194G= NP_000287.3:p.Cys4065=
NM_001009944.2:c.12197G= NP_001009944.2:p.Cys4066=
XM_005255370.2:c.9152G= XP_005255427.1:p.Cys3051=
XM_011522525.1:c.12275G= XP_011520827.1:p.Cys4092=
XM_011522526.1:c.12272G= XP_011520828.1:p.Cys4091=
XM_011522527.1:c.12257G= XP_011520829.1:p.Cys4086=
XM_011522528.1:c.12251G= XP_011520830.1:p.Cys4084=
XM_011522529.1:c.12248G= XP_011520831.1:p.Cys4083=
XM_011522530.1:c.12221G= XP_011520832.1:p.Cys4074=
XM_011522531.1:c.12203G= XP_011520833.1:p.Cys4068=
XM_011522532.1:c.12149G= XP_011520834.1:p.Cys4050=
XM_011522533.1:c.12068G= XP_011520835.1:p.Cys4023=
XM_011522534.1:c.12011G= XP_011520836.1:p.Cys4004=
XM_011522535.1:c.10097G= XP_011520837.1:p.Cys3366=
XM_011522537.1:c.9275G= XP_011520839.1:p.Cys3092=
XR_932867.1:n.12115G=
XM_005255370.3:c.9152G= XP_005255427.1:p.Cys3051=
XM_011522528.3:c.12251G= XP_011520830.1:p.Cys4084=
XM_011522529.2:c.12248G= XP_011520831.1:p.Cys4083=
XM_011522537.2:c.9275G= XP_011520839.1:p.Cys3092=
XM_024450298.1:c.12317G= XP_024306066.1:p.Cys4106=
XM_024450299.1:c.12245G= XP_024306067.1:p.Cys4082=
XM_024450300.1:c.12107G= XP_024306068.1:p.Cys4036=
XM_024450301.1:c.10193G= XP_024306069.1:p.Cys3398=
NM_000296.4:c.12194G= NP_000287.4:p.Cys4065=
NM_001009944.3:c.12197G= MANE Select NP_001009944.3:p.Cys4066=