Canonical Allele Identifier: CA16609233
Gene: DNAJC12 HGNC NCBI

Linked Data

ClinVar Variation Id: 393301
ClinVar RCV Id: RCV000445353
PubMed: PMID:28132689
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.67799813_67806755del , CM000672.2:g.67799813_67806755del GRCh38
NC_000010.10:g.69559571_69566513del , CM000672.1:g.69559571_69566513del GRCh37
NC_000010.9:g.69229577_69236519del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000225171.7:c.298-967_503-2602del
ENST00000225171.6:c.298-967_503-2602del
ENST00000483798.6:c.388-967_593-2602del
NM_021800.2:c.298-967_503-2602del
XM_011539967.1:c.328-967_533-2602del
XM_017016431.1:c.52-967_257-2602del
XM_017016432.2:c.52-967_257-2602del
NM_021800.3:c.298-967_503-2602del
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