Canonical Allele Identifier: CA11892689

Gene: PKD2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88038593A>G , CM000666.2:g.88038593A>G	GRCh38
NC_000004.11:g.88959745A>G , CM000666.1:g.88959745A>G	GRCh37
NC_000004.10:g.89178769A>G	NCBI36
NG_008604.1:g.35926A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000297.4:c.1094+92A>G MANE Select	NP_000288.1:n.1094+92A>G
ENST00000237596.7:c.1094+92A>G MANE Select	ENSP00000237596.2:n.1094+92A>G
NM_000297.3:c.1094+92A>G	NP_000288.1:n.1094+92A>G
NR_156488.1:n.1181+92A>G
NR_156488.2:n.1193+92A>G
ENST00000237596.6:c.1094+92A>G	ENSP00000237596.2:n.1094+92A>G
ENST00000506367.1:n.541+92A>G
XM_011532028.1:c.1094+92A>G	XP_011530330.1:n.1094+92A>G
XM_011532028.2:c.1094+92A>G	XP_011530330.1:n.1094+92A>G
XM_011532029.1:c.374+92A>G	XP_011530331.1:n.374+92A>G
XM_011532030.1:c.254+92A>G	XP_011530332.1:n.254+92A>G
XM_011532030.2:c.254+92A>G	XP_011530332.1:n.254+92A>G
XR_244632.2:n.1189+92A>G