Canonical Allele Identifier: CA16043405
Gene: PKD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 373955
dbSNP Id: rs1057518797

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88008090_88008097delinsTAGGACG , CM000666.2:g.88008090_88008097delinsTAGGACG GRCh38
NC_000004.11:g.88929242_88929249delinsTAGGACG , CM000666.1:g.88929242_88929249delinsTAGGACG GRCh37
NC_000004.10:g.89148266_89148273delinsTAGGACG NCBI36
NG_008604.1:g.5423_5430delinsTAGGACG

Transcript Alleles

HGVS Amino-acid change
ENST00000237596.7:c.357_364delinsTAGGACG MANE Select ENSP00000237596.2:p.Pro120ArgfsTer12
ENST00000237596.6:c.357_364delinsTAGGACG ENSP00000237596.2:p.Pro120ArgfsTer12
NM_000297.3:c.357_364delinsTAGGACG NP_000288.1:p.Pro120ArgfsTer12
XM_011532028.1:c.357_364delinsTAGGACG XP_011530330.1:p.Pro120ArgfsTer12
XR_244632.2:n.452_459delinsTAGGACG
NR_156488.1:n.444_451delinsTAGGACG
XM_011532028.2:c.357_364delinsTAGGACG XP_011530330.1:p.Pro120ArgfsTer12
NM_000297.4:c.357_364delinsTAGGACG MANE Select NP_000288.1:p.Pro120ArgfsTer12
NR_156488.2:n.456_463delinsTAGGACG