Canonical Allele Identifier: CA799592419

Gene: PKD2

Linked Data

• dbSNP Id: rs1210002606
• MyVariant Identifiers: chr4:g.88928825_88928827del (hg19) ; chr4:g.88007673_88007675del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88007673_88007675del , CM000666.2:g.88007673_88007675del	GRCh38
NC_000004.11:g.88928825_88928827del , CM000666.1:g.88928825_88928827del	GRCh37
NC_000004.10:g.89147849_89147851del	NCBI36
NG_008604.1:g.5006_5008del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.-61_-59del MANE Select	ENSP00000237596.2:n.-61_-59del
ENST00000237596.6:c.-61_-59del	ENSP00000237596.2:n.-61_-59del
NM_000297.3:c.-61_-59del	NP_000288.1:n.-61_-59del
XM_011532028.1:c.-61_-59del	XP_011530330.1:n.-61_-59del
XR_244632.2:n.35_37del
NR_156488.1:n.27_29del
XM_011532028.2:c.-61_-59del	XP_011530330.1:n.-61_-59del
NM_000297.4:c.-61_-59del MANE Select	NP_000288.1:n.-61_-59del
NR_156488.2:n.39_41del