Canonical Allele Identifier: CA367826342
Gene: DNAJC30 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73682966G>C , CM000669.2:g.73682966G>C GRCh38
NC_000007.13:g.73097296G>C , CM000669.1:g.73097296G>C GRCh37
NC_000007.12:g.72735232G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395176.3:c.458C>G MANE Select ENSP00000378605.1:p.Ala153Gly
ENST00000395176.2:c.458C>G ENSP00000378605.1:p.Ala153Gly
NM_032317.2:c.458C>G NP_115693.2:p.Ala153Gly
NM_032317.3:c.458C>G MANE Select NP_115693.2:p.Ala153Gly