Canonical Allele Identifier: CA5520870
Gene: DNAJC12 HGNC NCBI

Linked Data

dbSNP Id: rs369180417

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67811585C>T , CM000672.2:g.67811585C>T GRCh38
NC_000010.10:g.69571343C>T , CM000672.1:g.69571343C>T GRCh37
NC_000010.9:g.69241349C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000225171.7:c.236G>A MANE Select ENSP00000225171.2:p.Arg79Gln
ENST00000225171.6:c.236G>A ENSP00000225171.2:p.Arg79Gln
ENST00000339758.7:c.236G>A ENSP00000343575.6:p.Arg79Gln
ENST00000480180.1:c.*255G>A ENSP00000474804.1:n.*255G>A
ENST00000480963.5:c.*156G>A ENSP00000473979.1:n.*156G>A
ENST00000483798.6:c.326G>A ENSP00000474215.1:p.Arg109Gln
NM_021800.2:c.236G>A NP_068572.1:p.Arg79Gln
NM_201262.1:c.236G>A NP_957714.1:p.Arg79Gln
XM_011539967.1:c.266G>A XP_011538269.1:p.Arg89Gln
XM_017016431.1:c.-11G>A XP_016871920.1:n.-11G>A
XM_017016432.2:c.-11G>A XP_016871921.1:n.-11G>A
NM_021800.3:c.236G>A MANE Select NP_068572.1:p.Arg79Gln
NM_201262.2:c.236G>A NP_957714.1:p.Arg79Gln