Canonical Allele Identifier: CA2578140542
Gene: PKD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88046878T>G , CM000666.2:g.88046878T>G GRCh38
NC_000004.11:g.88968030T>G , CM000666.1:g.88968030T>G GRCh37
NC_000004.10:g.89187054T>G NCBI36
NG_008604.1:g.44211T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.1548+8T>G MANE Select ENSP00000237596.2:n.1548+8T>G
ENST00000237596.6:c.1548+8T>G ENSP00000237596.2:n.1548+8T>G
ENST00000508588.5:c.-199+3421T>G ENSP00000427131.1:n.-199+3421T>G
NM_000297.3:c.1548+8T>G NP_000288.1:n.1548+8T>G
XM_011532028.1:c.1323+8T>G XP_011530330.1:n.1323+8T>G
XM_011532029.1:c.828+8T>G XP_011530331.1:n.828+8T>G
XM_011532030.1:c.708+8T>G XP_011530332.1:n.708+8T>G
XR_244632.2:n.1643+8T>G
NR_156488.1:n.1635+8T>G
XM_011532028.2:c.1323+8T>G XP_011530330.1:n.1323+8T>G
XM_011532030.2:c.708+8T>G XP_011530332.1:n.708+8T>G
NM_000297.4:c.1548+8T>G MANE Select NP_000288.1:n.1548+8T>G
NR_156488.2:n.1647+8T>G