Canonical Allele Identifier: CA1474562581

Gene: PKD2

Linked Data

• dbSNP Id: rs1726275489

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88008536_88008537insGGG , CM000666.2:g.88008536_88008537insGGG	GRCh38
NC_000004.11:g.88929688_88929689insGGG , CM000666.1:g.88929688_88929689insGGG	GRCh37
NC_000004.10:g.89148712_89148713insGGG	NCBI36
NG_008604.1:g.5869_5870insGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237596.7:c.595+208_595+209insGGG MANE Select	ENSP00000237596.2:n.595+208_595+209insGGG
ENST00000237596.6:c.595+208_595+209insGGG	ENSP00000237596.2:n.595+208_595+209insGGG
ENST00000506727.1:n.97+208_97+209insGGG
NM_000297.3:c.595+208_595+209insGGG	NP_000288.1:n.595+208_595+209insGGG
XM_011532028.1:c.595+208_595+209insGGG	XP_011530330.1:n.595+208_595+209insGGG
XR_244632.2:n.690+208_690+209insGGG
NR_156488.1:n.682+208_682+209insGGG
XM_011532028.2:c.595+208_595+209insGGG	XP_011530330.1:n.595+208_595+209insGGG
NM_000297.4:c.595+208_595+209insGGG MANE Select	NP_000288.1:n.595+208_595+209insGGG
NR_156488.2:n.694+208_694+209insGGG