Canonical Allele Identifier: CA1474575843
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88038391_88038392delinsTG , CM000666.2:g.88038391_88038392delinsTG GRCh38
NC_000004.11:g.88959543_88959544delinsTG , CM000666.1:g.88959543_88959544delinsTG GRCh37
NC_000004.10:g.89178567_89178568delinsTG NCBI36
NG_008604.1:g.35724_35725delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000237596.7:c.984_985delinsTG MANE Select ENSP00000237596.2:p.Asn328=
ENST00000237596.6:c.984_985delinsTG ENSP00000237596.2:p.Asn328=
ENST00000506367.1:n.431_432delinsTG
NM_000297.3:c.984_985delinsTG NP_000288.1:p.Asn328=
XM_011532028.1:c.984_985delinsTG XP_011530330.1:p.Asn328=
XM_011532029.1:c.264_265delinsTG XP_011530331.1:p.Asn88=
XM_011532030.1:c.144_145delinsTG XP_011530332.1:p.Asn48=
XR_244632.2:n.1079_1080delinsTG
NR_156488.1:n.1071_1072delinsTG
XM_011532028.2:c.984_985delinsTG XP_011530330.1:p.Asn328=
XM_011532030.2:c.144_145delinsTG XP_011530332.1:p.Asn48=
NM_000297.4:c.984_985delinsTG MANE Select NP_000288.1:p.Asn328=
NR_156488.2:n.1083_1084delinsTG