Canonical Allele Identifier: CA3003777
Community Standard Title: NM_000297.4(PKD2):c.710-11C>A
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88036209C>A , CM000666.2:g.88036209C>A GRCh38
NC_000004.11:g.88957361C>A , CM000666.1:g.88957361C>A GRCh37
NC_000004.10:g.89176385C>A NCBI36
NG_008604.1:g.33542C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000297.4:c.710-11C>A MANE Select NP_000288.1:n.710-11C>A
ENST00000237596.7:c.710-11C>A MANE Select ENSP00000237596.2:n.710-11C>A
NM_000297.3:c.710-11C>A NP_000288.1:n.710-11C>A
NR_156488.1:n.797-11C>A
NR_156488.2:n.809-11C>A
ENST00000237596.6:c.710-11C>A ENSP00000237596.2:n.710-11C>A
ENST00000506367.1:n.146C>A
ENST00000506727.1:n.285C>A
XM_011532028.1:c.710-11C>A XP_011530330.1:n.710-11C>A
XM_011532028.2:c.710-11C>A XP_011530330.1:n.710-11C>A
XM_011532029.1:c.-11-11C>A XP_011530331.1:n.-11-11C>A
XR_244632.2:n.805-11C>A