Canonical Allele Identifier: CA1717166255
Gene: DNAJC30 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73682994T= , CM000669.2:g.73682994T= GRCh38
NC_000007.13:g.73097324T= , CM000669.1:g.73097324T= GRCh37
NC_000007.12:g.72735260T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395176.3:c.430A= MANE Select ENSP00000378605.1:p.Thr144=
ENST00000395176.2:c.430A= ENSP00000378605.1:p.Thr144=
NM_032317.2:c.430A= NP_115693.2:p.Thr144=
NM_032317.3:c.430A= MANE Select NP_115693.2:p.Thr144=