Canonical Allele Identifier: CA1917049476
Gene: DNAJC12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67811581C= , CM000672.2:g.67811581C= GRCh38
NC_000010.10:g.69571339C= , CM000672.1:g.69571339C= GRCh37
NC_000010.9:g.69241345C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000225171.7:c.240G= MANE Select ENSP00000225171.2:p.Arg80=
ENST00000225171.6:c.240G= ENSP00000225171.2:p.Arg80=
ENST00000339758.7:c.240G= ENSP00000343575.6:p.Arg80=
ENST00000480180.1:c.*259G= ENSP00000474804.1:n.*259G=
ENST00000480963.5:c.*160G= ENSP00000473979.1:n.*160G=
ENST00000483798.6:c.330G= ENSP00000474215.1:p.Arg110=
NM_021800.2:c.240G= NP_068572.1:p.Arg80=
NM_201262.1:c.240G= NP_957714.1:p.Arg80=
XM_011539967.1:c.270G= XP_011538269.1:p.Arg90=
XM_017016431.1:c.-7G= XP_016871920.1:n.-7G=
XM_017016432.2:c.-7G= XP_016871921.1:n.-7G=
NM_021800.3:c.240G= MANE Select NP_068572.1:p.Arg80=
NM_201262.2:c.240G= NP_957714.1:p.Arg80=