Canonical Allele Identifier: CA1717166263
Gene: DNAJC30 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73683006T= , CM000669.2:g.73683006T= GRCh38
NC_000007.13:g.73097336T= , CM000669.1:g.73097336T= GRCh37
NC_000007.12:g.72735272T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395176.3:c.418A= MANE Select ENSP00000378605.1:p.Thr140=
ENST00000395176.2:c.418A= ENSP00000378605.1:p.Thr140=
NM_032317.2:c.418A= NP_115693.2:p.Thr140=
NM_032317.3:c.418A= MANE Select NP_115693.2:p.Thr140=
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