Canonical Allele Identifier: CA2578140573
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88046957T>C , CM000666.2:g.88046957T>C GRCh38
NC_000004.11:g.88968109T>C , CM000666.1:g.88968109T>C GRCh37
NC_000004.10:g.89187133T>C NCBI36
NG_008604.1:g.44290T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.1548+87T>C MANE Select ENSP00000237596.2:n.1548+87T>C
ENST00000237596.6:c.1548+87T>C ENSP00000237596.2:n.1548+87T>C
ENST00000508588.5:c.-199+3500T>C ENSP00000427131.1:n.-199+3500T>C
NM_000297.3:c.1548+87T>C NP_000288.1:n.1548+87T>C
XM_011532028.1:c.1323+87T>C XP_011530330.1:n.1323+87T>C
XM_011532029.1:c.828+87T>C XP_011530331.1:n.828+87T>C
XM_011532030.1:c.708+87T>C XP_011530332.1:n.708+87T>C
XR_244632.2:n.1643+87T>C
NR_156488.1:n.1635+87T>C
XM_011532028.2:c.1323+87T>C XP_011530330.1:n.1323+87T>C
XM_011532030.2:c.708+87T>C XP_011530332.1:n.708+87T>C
NM_000297.4:c.1548+87T>C MANE Select NP_000288.1:n.1548+87T>C
NR_156488.2:n.1647+87T>C