Canonical Allele Identifier: CA357618625
Gene: PKD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88046686G>T , CM000666.2:g.88046686G>T GRCh38
NC_000004.11:g.88967838G>T , CM000666.1:g.88967838G>T GRCh37
NC_000004.10:g.89186862G>T NCBI36
NG_008604.1:g.44019G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000237596.7:c.1364G>T MANE Select ENSP00000237596.2:p.Trp455Leu
ENST00000237596.6:c.1364G>T ENSP00000237596.2:p.Trp455Leu
ENST00000508588.5:c.-199+3229G>T ENSP00000427131.1:n.-199+3229G>T
NM_000297.3:c.1364G>T NP_000288.1:p.Trp455Leu
XM_011532028.1:c.1139G>T XP_011530330.1:p.Trp380Leu
XM_011532029.1:c.644G>T XP_011530331.1:p.Trp215Leu
XM_011532030.1:c.524G>T XP_011530332.1:p.Trp175Leu
XR_244632.2:n.1459G>T
NR_156488.1:n.1451G>T
XM_011532028.2:c.1139G>T XP_011530330.1:p.Trp380Leu
XM_011532030.2:c.524G>T XP_011530332.1:p.Trp175Leu
NM_000297.4:c.1364G>T MANE Select NP_000288.1:p.Trp455Leu
NR_156488.2:n.1463G>T