Canonical Allele Identifier: CA2202042063
Gene: PKD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2090557C= , CM000678.2:g.2090557C= GRCh38
NC_000016.9:g.2140558C= , CM000678.1:g.2140558C= GRCh37
NC_000016.8:g.2080559C= NCBI36
NG_005895.1:g.46252C= , LRG_487:g.46252C=
NG_008617.1:g.52664G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.12172G= MANE Select ENSP00000262304.4:p.Val4058=
ENST00000262304.8:c.12172G= ENSP00000262304.4:p.Val4058=
ENST00000423118.5:c.12169G= ENSP00000399501.1:p.Val4057=
ENST00000472577.1:n.200G=
NM_000296.3:c.12169G= NP_000287.3:p.Val4057=
NM_001009944.2:c.12172G= NP_001009944.2:p.Val4058=
XM_005255370.2:c.9127G= XP_005255427.1:p.Val3043=
XM_011522525.1:c.12250G= XP_011520827.1:p.Val4084=
XM_011522526.1:c.12247G= XP_011520828.1:p.Val4083=
XM_011522527.1:c.12232G= XP_011520829.1:p.Val4078=
XM_011522528.1:c.12226G= XP_011520830.1:p.Val4076=
XM_011522529.1:c.12223G= XP_011520831.1:p.Val4075=
XM_011522530.1:c.12196G= XP_011520832.1:p.Val4066=
XM_011522531.1:c.12178G= XP_011520833.1:p.Val4060=
XM_011522532.1:c.12124G= XP_011520834.1:p.Val4042=
XM_011522533.1:c.12043G= XP_011520835.1:p.Val4015=
XM_011522534.1:c.11986G= XP_011520836.1:p.Val3996=
XM_011522535.1:c.10072G= XP_011520837.1:p.Val3358=
XM_011522537.1:c.9250G= XP_011520839.1:p.Val3084=
XR_932867.1:n.12090G=
XM_005255370.3:c.9127G= XP_005255427.1:p.Val3043=
XM_011522528.3:c.12226G= XP_011520830.1:p.Val4076=
XM_011522529.2:c.12223G= XP_011520831.1:p.Val4075=
XM_011522537.2:c.9250G= XP_011520839.1:p.Val3084=
XM_024450298.1:c.12292G= XP_024306066.1:p.Val4098=
XM_024450299.1:c.12220G= XP_024306067.1:p.Val4074=
XM_024450300.1:c.12082G= XP_024306068.1:p.Val4028=
XM_024450301.1:c.10168G= XP_024306069.1:p.Val3390=
NM_000296.4:c.12169G= NP_000287.4:p.Val4057=
NM_001009944.3:c.12172G= MANE Select NP_001009944.3:p.Val4058=