Canonical Allele Identifier: CA1917049474
Gene: DNAJC12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67811577G= , CM000672.2:g.67811577G= GRCh38
NC_000010.10:g.69571335G= , CM000672.1:g.69571335G= GRCh37
NC_000010.9:g.69241341G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000225171.7:c.244C= MANE Select ENSP00000225171.2:p.Gln82=
ENST00000225171.6:c.244C= ENSP00000225171.2:p.Gln82=
ENST00000339758.7:c.244C= ENSP00000343575.6:p.Gln82=
ENST00000480180.1:c.*263C= ENSP00000474804.1:n.*263C=
ENST00000480963.5:c.*164C= ENSP00000473979.1:n.*164C=
ENST00000483798.6:c.334C= ENSP00000474215.1:p.Gln112=
NM_021800.2:c.244C= NP_068572.1:p.Gln82=
NM_201262.1:c.244C= NP_957714.1:p.Gln82=
XM_011539967.1:c.274C= XP_011538269.1:p.Gln92=
XM_017016431.1:c.-3C= XP_016871920.1:n.-3C=
XM_017016432.2:c.-3C= XP_016871921.1:n.-3C=
NM_021800.3:c.244C= MANE Select NP_068572.1:p.Gln82=
NM_201262.2:c.244C= NP_957714.1:p.Gln82=