Canonical Allele Identifier: CA357630870
Community Standard Title: NM_000297.4(PKD2):c.710-1G>A
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88036219G>A , CM000666.2:g.88036219G>A GRCh38
NC_000004.11:g.88957371G>A , CM000666.1:g.88957371G>A GRCh37
NC_000004.10:g.89176395G>A NCBI36
NG_008604.1:g.33552G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000297.4:c.710-1G>A MANE Select NP_000288.1:n.710-1G>A
ENST00000237596.7:c.710-1G>A MANE Select ENSP00000237596.2:n.710-1G>A
NM_000297.3:c.710-1G>A NP_000288.1:n.710-1G>A
NR_156488.1:n.797-1G>A
NR_156488.2:n.809-1G>A
ENST00000237596.6:c.710-1G>A ENSP00000237596.2:n.710-1G>A
ENST00000506367.1:n.156G>A
ENST00000506727.1:n.295G>A
XM_011532028.1:c.710-1G>A XP_011530330.1:n.710-1G>A
XM_011532028.2:c.710-1G>A XP_011530330.1:n.710-1G>A
XM_011532029.1:c.-11-1G>A XP_011530331.1:n.-11-1G>A
XR_244632.2:n.805-1G>A