Canonical Allele Identifier: CA1717166259
Gene: DNAJC30 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73682999G= , CM000669.2:g.73682999G= GRCh38
NC_000007.13:g.73097329G= , CM000669.1:g.73097329G= GRCh37
NC_000007.12:g.72735265G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395176.3:c.425C= MANE Select ENSP00000378605.1:p.Pro142=
ENST00000395176.2:c.425C= ENSP00000378605.1:p.Pro142=
NM_032317.2:c.425C= NP_115693.2:p.Pro142=
NM_032317.3:c.425C= MANE Select NP_115693.2:p.Pro142=