Canonical Allele Identifier: CA2609360328
Gene: DNAJC12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67811441_67811443del , CM000672.2:g.67811441_67811443del GRCh38
NC_000010.10:g.69571199_69571201del , CM000672.1:g.69571199_69571201del GRCh37
NC_000010.9:g.69241205_69241207del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000225171.7:c.297+82_297+84del MANE Select ENSP00000225171.2:n.297+82_297+84del
ENST00000225171.6:c.297+82_297+84del ENSP00000225171.2:n.297+82_297+84del
ENST00000339758.7:c.*55_*57del ENSP00000343575.6:n.*55_*57del
ENST00000480963.5:c.*217+82_*217+84del ENSP00000473979.1:n.*217+82_*217+84del
ENST00000483798.6:c.387+82_387+84del ENSP00000474215.1:n.387+82_387+84del
NM_021800.2:c.297+82_297+84del NP_068572.1:n.297+82_297+84del
NM_201262.1:c.*55_*57del NP_957714.1:n.*55_*57del
XM_011539967.1:c.327+82_327+84del XP_011538269.1:n.327+82_327+84del
XM_017016431.1:c.51+82_51+84del XP_016871920.1:n.51+82_51+84del
XM_017016432.2:c.51+82_51+84del XP_016871921.1:n.51+82_51+84del
NM_021800.3:c.297+82_297+84del MANE Select NP_068572.1:n.297+82_297+84del
NM_201262.2:c.*55_*57del NP_957714.1:n.*55_*57del