Canonical Allele Identifier: CA1917049498
Gene: DNAJC12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67811607G= , CM000672.2:g.67811607G= GRCh38
NC_000010.10:g.69571365G= , CM000672.1:g.69571365G= GRCh37
NC_000010.9:g.69241371G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000225171.7:c.214C= MANE Select ENSP00000225171.2:p.Arg72=
ENST00000225171.6:c.214C= ENSP00000225171.2:p.Arg72=
ENST00000339758.7:c.214C= ENSP00000343575.6:p.Arg72=
ENST00000480180.1:c.*233C= ENSP00000474804.1:n.*233C=
ENST00000480963.5:c.*134C= ENSP00000473979.1:n.*134C=
ENST00000483798.6:c.304C= ENSP00000474215.1:p.Arg102=
NM_021800.2:c.214C= NP_068572.1:p.Arg72=
NM_201262.1:c.214C= NP_957714.1:p.Arg72=
XM_011539967.1:c.244C= XP_011538269.1:p.Arg82=
XM_017016431.1:c.-33C= XP_016871920.1:n.-33C=
XM_017016432.2:c.-33C= XP_016871921.1:n.-33C=
NM_021800.3:c.214C= MANE Select NP_068572.1:p.Arg72=
NM_201262.2:c.214C= NP_957714.1:p.Arg72=