Canonical Allele Identifier: CA367826682

Gene: DNAJC30

Linked Data

• MyVariant Identifiers: chr7:g.73097351G>C (hg19) ; chr7:g.73683021G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.73683021G>C , CM000669.2:g.73683021G>C	GRCh38
NC_000007.13:g.73097351G>C , CM000669.1:g.73097351G>C	GRCh37
NC_000007.12:g.72735287G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395176.3:c.403C>G MANE Select	ENSP00000378605.1:p.Pro135Ala
ENST00000395176.2:c.403C>G	ENSP00000378605.1:p.Pro135Ala
NM_032317.2:c.403C>G	NP_115693.2:p.Pro135Ala
NM_032317.3:c.403C>G MANE Select	NP_115693.2:p.Pro135Ala