Canonical Allele Identifier: CA493049706

Gene: PKD1

Linked Data

• dbSNP Id: rs759156296
• gnomAD v2: 16-2165448-G-C
• gnomAD v4: 16-2115447-G-C
• MyVariant Identifiers: chr16:g.2165448G>C (hg19) ; chr16:g.2115447G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2115447G>C , CM000678.2:g.2115447G>C	GRCh38
NC_000016.9:g.2165448G>C , CM000678.1:g.2165448G>C	GRCh37
NC_000016.8:g.2105449G>C	NCBI36
NG_008617.1:g.25452C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.2028C>G MANE Select	ENSP00000262304.4:p.Pro676=
ENST00000262304.8:c.2028C>G	ENSP00000262304.4:p.Pro676=
ENST00000423118.5:c.2028C>G	ENSP00000399501.1:p.Pro676=
ENST00000488185.2:c.472+2042C>G
ENST00000568591.5:c.959C>G	ENSP00000457162.1:n.959C>G
NM_000296.3:c.2028C>G	NP_000287.3:p.Pro676=
NM_001009944.2:c.2028C>G	NP_001009944.2:p.Pro676=
XM_011522525.1:c.2082C>G	XP_011520827.1:p.Pro694=
XM_011522526.1:c.2082C>G	XP_011520828.1:p.Pro694=
XM_011522527.1:c.2082C>G	XP_011520829.1:p.Pro694=
XM_011522528.1:c.2082C>G	XP_011520830.1:p.Pro694=
XM_011522529.1:c.2082C>G	XP_011520831.1:p.Pro694=
XM_011522530.1:c.2028C>G	XP_011520832.1:p.Pro676=
XM_011522531.1:c.2010C>G	XP_011520833.1:p.Pro670=
XM_011522532.1:c.1956C>G	XP_011520834.1:p.Pro652=
XM_011522533.1:c.1875C>G	XP_011520835.1:p.Pro625=
XM_011522534.1:c.1818C>G	XP_011520836.1:p.Pro606=
XM_011522536.1:c.2082C>G	XP_011520838.1:p.Pro694=
XR_932867.1:n.2097C>G
XR_932868.1:n.2097C>G
XR_932869.1:n.2097C>G
XR_932870.1:n.2097C>G
XM_011522528.3:c.2082C>G	XP_011520830.1:p.Pro694=
XM_011522529.2:c.2082C>G	XP_011520831.1:p.Pro694=
XM_024450298.1:c.2028C>G	XP_024306066.1:p.Pro676=
XM_024450299.1:c.1956C>G	XP_024306067.1:p.Pro652=
XM_024450300.1:c.1818C>G	XP_024306068.1:p.Pro606=
NM_000296.4:c.2028C>G	NP_000287.4:p.Pro676=
NM_001009944.3:c.2028C>G MANE Select	NP_001009944.3:p.Pro676=