Canonical Allele Identifier: CA1917049452
Gene: DNAJC12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67811527C= , CM000672.2:g.67811527C= GRCh38
NC_000010.10:g.69571285C= , CM000672.1:g.69571285C= GRCh37
NC_000010.9:g.69241291C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000225171.7:c.294G= MANE Select ENSP00000225171.2:p.Lys98=
ENST00000225171.6:c.294G= ENSP00000225171.2:p.Lys98=
ENST00000339758.7:c.294G= ENSP00000343575.6:p.Lys98=
ENST00000480963.5:c.*214G= ENSP00000473979.1:n.*214G=
ENST00000483798.6:c.384G= ENSP00000474215.1:p.Lys128=
NM_021800.2:c.294G= NP_068572.1:p.Lys98=
NM_201262.1:c.294G= NP_957714.1:p.Lys98=
XM_011539967.1:c.324G= XP_011538269.1:p.Lys108=
XM_017016431.1:c.48G= XP_016871920.1:p.Lys16=
XM_017016432.2:c.48G= XP_016871921.1:p.Lys16=
NM_021800.3:c.294G= MANE Select NP_068572.1:p.Lys98=
NM_201262.2:c.294G= NP_957714.1:p.Lys98=