Canonical Allele Identifier: CA367826371
Gene: DNAJC30 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73682972G>A , CM000669.2:g.73682972G>A GRCh38
NC_000007.13:g.73097302G>A , CM000669.1:g.73097302G>A GRCh37
NC_000007.12:g.72735238G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395176.3:c.452C>T MANE Select ENSP00000378605.1:p.Ser151Phe
ENST00000395176.2:c.452C>T ENSP00000378605.1:p.Ser151Phe
NM_032317.2:c.452C>T NP_115693.2:p.Ser151Phe
NM_032317.3:c.452C>T MANE Select NP_115693.2:p.Ser151Phe