Canonical Allele Identifier: CA492962447
Gene: PKD1 HGNC NCBI
PKD1-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.2142512G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2092511G>T , CM000678.2:g.2092511G>T GRCh38
NC_000016.9:g.2142512G>T , CM000678.1:g.2142512G>T GRCh37
NC_000016.8:g.2082513G>T NCBI36
NG_008617.1:g.50710C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.11238C>A (PKD1) MANE Select ENSP00000262304.4:p.Pro3746=
ENST00000262304.8:c.11238C>A (PKD1) ENSP00000262304.4:p.Pro3746=
ENST00000423118.5:c.11235C>A (PKD1) ENSP00000399501.1:p.Pro3745=
ENST00000485120.1:n.87C>A (PKD1)
ENST00000487932.5:c.5800C>A (PKD1) ENSP00000457132.1:n.5800C>A
ENST00000562425.1:c.351C>A (PKD1)
ENST00000567355.1:n.401C>A (PKD1)
NM_000296.3:c.11235C>A (PKD1) NP_000287.3:p.Pro3745=
NM_001009944.2:c.11238C>A (PKD1) NP_001009944.2:p.Pro3746=
XM_005255370.2:c.8193C>A (PKD1) XP_005255427.1:p.Pro2731=
XM_011522525.1:c.11316C>A (PKD1) XP_011520827.1:p.Pro3772=
XM_011522526.1:c.11313C>A (PKD1) XP_011520828.1:p.Pro3771=
XM_011522527.1:c.11298C>A (PKD1) XP_011520829.1:p.Pro3766=
XM_011522528.1:c.11292C>A (PKD1) XP_011520830.1:p.Pro3764=
XM_011522529.1:c.11289C>A (PKD1) XP_011520831.1:p.Pro3763=
XM_011522530.1:c.11262C>A (PKD1) XP_011520832.1:p.Pro3754=
XM_011522531.1:c.11244C>A (PKD1) XP_011520833.1:p.Pro3748=
XM_011522532.1:c.11190C>A (PKD1) XP_011520834.1:p.Pro3730=
XM_011522533.1:c.11109C>A (PKD1) XP_011520835.1:p.Pro3703=
XM_011522534.1:c.11052C>A (PKD1) XP_011520836.1:p.Pro3684=
XM_011522535.1:c.9138C>A (PKD1) XP_011520837.1:p.Pro3046=
XM_011522537.1:c.8316C>A (PKD1) XP_011520839.1:p.Pro2772=
XR_932867.1:n.11331C>A (PKD1)
XR_932868.1:n.11110-323C>A (PKD1)
XR_932869.1:n.11110-323C>A (PKD1)
XR_932870.1:n.11191C>A (PKD1)
XR_933000.1:n.90-378G>T (PKD1-AS1)
XR_933001.1:n.180-378G>T (PKD1-AS1)
XR_933002.1:n.89-378G>T (PKD1-AS1)
XR_933003.1:n.89-378G>T (PKD1-AS1)
NR_135175.1:n.180-378G>T (PKD1-AS1)
XM_005255370.3:c.8193C>A (PKD1) XP_005255427.1:p.Pro2731=
XM_011522528.3:c.11292C>A (PKD1) XP_011520830.1:p.Pro3764=
XM_011522529.2:c.11289C>A (PKD1) XP_011520831.1:p.Pro3763=
XM_011522537.2:c.8316C>A (PKD1) XP_011520839.1:p.Pro2772=
XM_024450298.1:c.11358C>A (PKD1) XP_024306066.1:p.Pro3786=
XM_024450299.1:c.11286C>A (PKD1) XP_024306067.1:p.Pro3762=
XM_024450300.1:c.11148C>A (PKD1) XP_024306068.1:p.Pro3716=
XM_024450301.1:c.9234C>A (PKD1) XP_024306069.1:p.Pro3078=
NM_000296.4:c.11235C>A (PKD1) NP_000287.4:p.Pro3745=
NM_001009944.3:c.11238C>A (PKD1) MANE Select NP_001009944.3:p.Pro3746=