Canonical Allele Identifier: CA1917049497
Gene: DNAJC12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67811606C= , CM000672.2:g.67811606C= GRCh38
NC_000010.10:g.69571364C= , CM000672.1:g.69571364C= GRCh37
NC_000010.9:g.69241370C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_021800.3:c.215G= MANE Select NP_068572.1:p.Arg72=
ENST00000225171.7:c.215G= MANE Select ENSP00000225171.2:p.Arg72=
NM_021800.2:c.215G= NP_068572.1:p.Arg72=
NM_201262.1:c.215G= NP_957714.1:p.Arg72=
NM_201262.2:c.215G= NP_957714.1:p.Arg72=
ENST00000225171.6:c.215G= ENSP00000225171.2:p.Arg72=
ENST00000339758.7:c.215G= ENSP00000343575.6:p.Arg72=
ENST00000480180.1:c.*234G= ENSP00000474804.1:n.*234G=
ENST00000480963.5:c.*135G= ENSP00000473979.1:n.*135G=
ENST00000483798.6:c.305G= ENSP00000474215.1:p.Arg102=
XM_011539967.1:c.245G= XP_011538269.1:p.Arg82=
XM_017016431.1:c.-32G= XP_016871920.1:n.-32G=
XM_017016432.2:c.-32G= XP_016871921.1:n.-32G=