Canonical Allele Identifier: CA406490178
Gene: PRKD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.46704645G>C , CM000681.2:g.46704645G>C GRCh38
NC_000019.9:g.47207902G>C , CM000681.1:g.47207902G>C GRCh37
NC_000019.8:g.51899742G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000291281.9:c.516C>G MANE Select ENSP00000291281.3:p.Cys172Trp
ENST00000291281.8:c.516C>G ENSP00000291281.3:p.Cys172Trp
ENST00000433867.5:c.516C>G ENSP00000393978.1:p.Cys172Trp
ENST00000595132.5:c.45C>G ENSP00000470363.1:p.Cys15Trp
ENST00000595515.5:c.516C>G ENSP00000470804.1:p.Cys172Trp
ENST00000597641.1:c.251C>G ENSP00000469064.1:n.251C>G
ENST00000598633.1:c.45C>G ENSP00000470919.1:p.Cys15Trp
ENST00000600194.5:c.45C>G ENSP00000472744.1:p.Cys15Trp
ENST00000601605.5:c.41-3533C>G ENSP00000470442.1:n.41-3533C>G
ENST00000601806.5:c.45C>G ENSP00000469106.1:p.Cys15Trp
NM_001079880.1:c.516C>G NP_001073349.1:p.Cys172Trp
NM_001079881.1:c.516C>G NP_001073350.1:p.Cys172Trp
NM_001079882.1:c.45C>G NP_001073351.1:p.Cys15Trp
NM_016457.4:c.516C>G NP_057541.2:p.Cys172Trp
XM_005258716.2:c.45C>G XP_005258773.2:p.Cys15Trp
NM_001079880.2:c.516C>G NP_001073349.1:p.Cys172Trp
NM_001079881.2:c.516C>G NP_001073350.1:p.Cys172Trp
NM_001079882.2:c.45C>G NP_001073351.1:p.Cys15Trp
NM_016457.5:c.516C>G MANE Select NP_057541.2:p.Cys172Trp