Canonical Allele Identifier: CA2578140606
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88038234G>A , CM000666.2:g.88038234G>A GRCh38
NC_000004.11:g.88959386G>A , CM000666.1:g.88959386G>A GRCh37
NC_000004.10:g.89178410G>A NCBI36
NG_008604.1:g.35567G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.844-17G>A MANE Select ENSP00000237596.2:n.844-17G>A
ENST00000237596.6:c.844-17G>A ENSP00000237596.2:n.844-17G>A
ENST00000506367.1:n.291-17G>A
ENST00000506727.1:n.430-17G>A
NM_000297.3:c.844-17G>A NP_000288.1:n.844-17G>A
XM_011532028.1:c.844-17G>A XP_011530330.1:n.844-17G>A
XM_011532029.1:c.124-17G>A XP_011530331.1:n.124-17G>A
XM_011532030.1:c.4-17G>A XP_011530332.1:n.4-17G>A
XR_244632.2:n.939-17G>A
NR_156488.1:n.931-17G>A
XM_011532028.2:c.844-17G>A XP_011530330.1:n.844-17G>A
XM_011532030.2:c.4-17G>A XP_011530332.1:n.4-17G>A
NM_000297.4:c.844-17G>A MANE Select NP_000288.1:n.844-17G>A
NR_156488.2:n.943-17G>A