Canonical Allele Identifier: CA7833161

Gene: PKD1

Linked Data

• ClinVar Variation Id: 3213456
• ClinVar RCV Id: RCV004506359
• dbSNP Id: rs761489072
• ExAC: 16:2164439 G / C
• gnomAD v2: 16-2164439-G-C
• gnomAD v3: 16-2114438-G-C
• gnomAD v4: 16-2114438-G-C
• MyVariant Identifiers: chr16:g.2164439G>C (hg19) ; chr16:g.2114438G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2114438G>C , CM000678.2:g.2114438G>C	GRCh38
NC_000016.9:g.2164439G>C , CM000678.1:g.2164439G>C	GRCh37
NC_000016.8:g.2104440G>C	NCBI36
NG_008617.1:g.26461C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.2585C>G MANE Select	ENSP00000262304.4:p.Pro862Arg
ENST00000262304.8:c.2585C>G	ENSP00000262304.4:p.Pro862Arg
ENST00000423118.5:c.2585C>G	ENSP00000399501.1:p.Pro862Arg
ENST00000488185.2:c.472+3051C>G
ENST00000565639.6:n.44C>G
ENST00000568591.5:c.1516C>G	ENSP00000457162.1:n.1516C>G
NM_000296.3:c.2585C>G	NP_000287.3:p.Pro862Arg
NM_001009944.2:c.2585C>G	NP_001009944.2:p.Pro862Arg
XM_011522525.1:c.2639C>G	XP_011520827.1:p.Pro880Arg
XM_011522526.1:c.2639C>G	XP_011520828.1:p.Pro880Arg
XM_011522527.1:c.2639C>G	XP_011520829.1:p.Pro880Arg
XM_011522528.1:c.2639C>G	XP_011520830.1:p.Pro880Arg
XM_011522529.1:c.2639C>G	XP_011520831.1:p.Pro880Arg
XM_011522530.1:c.2585C>G	XP_011520832.1:p.Pro862Arg
XM_011522531.1:c.2567C>G	XP_011520833.1:p.Pro856Arg
XM_011522532.1:c.2513C>G	XP_011520834.1:p.Pro838Arg
XM_011522533.1:c.2432C>G	XP_011520835.1:p.Pro811Arg
XM_011522534.1:c.2375C>G	XP_011520836.1:p.Pro792Arg
XM_011522535.1:c.461C>G	XP_011520837.1:p.Pro154Arg
XM_011522536.1:c.2639C>G	XP_011520838.1:p.Pro880Arg
XR_932867.1:n.2654C>G
XR_932868.1:n.2654C>G
XR_932869.1:n.2654C>G
XR_932870.1:n.2654C>G
XM_005255370.3:c.-465C>G	XP_005255427.1:n.-465C>G
XM_011522528.3:c.2639C>G	XP_011520830.1:p.Pro880Arg
XM_011522529.2:c.2639C>G	XP_011520831.1:p.Pro880Arg
XM_024450298.1:c.2585C>G	XP_024306066.1:p.Pro862Arg
XM_024450299.1:c.2513C>G	XP_024306067.1:p.Pro838Arg
XM_024450300.1:c.2375C>G	XP_024306068.1:p.Pro792Arg
XM_024450301.1:c.461C>G	XP_024306069.1:p.Pro154Arg
NM_000296.4:c.2585C>G	NP_000287.4:p.Pro862Arg
NM_001009944.3:c.2585C>G MANE Select	NP_001009944.3:p.Pro862Arg