Canonical Allele Identifier: CA594239135

Gene: DNAJC12

Linked Data

• dbSNP Id: rs1216349982
• gnomAD v2: 10-69571200-G-C
• gnomAD v3: 10-67811442-G-C
• gnomAD v4: 10-67811442-G-C
• MyVariant Identifiers: chr10:g.69571200G>C (hg19) ; chr10:g.67811442G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811442G>C , CM000672.2:g.67811442G>C	GRCh38
NC_000010.10:g.69571200G>C , CM000672.1:g.69571200G>C	GRCh37
NC_000010.9:g.69241206G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.297+82C>G MANE Select	ENSP00000225171.2:n.297+82C>G
ENST00000225171.6:c.297+82C>G	ENSP00000225171.2:n.297+82C>G
ENST00000339758.7:c.*55C>G	ENSP00000343575.6:n.*55C>G
ENST00000480963.5:c.*217+82C>G	ENSP00000473979.1:n.*217+82C>G
ENST00000483798.6:c.387+82C>G	ENSP00000474215.1:n.387+82C>G
NM_021800.2:c.297+82C>G	NP_068572.1:n.297+82C>G
NM_201262.1:c.*55C>G	NP_957714.1:n.*55C>G
XM_011539967.1:c.327+82C>G	XP_011538269.1:n.327+82C>G
XM_017016431.1:c.51+82C>G	XP_016871920.1:n.51+82C>G
XM_017016432.2:c.51+82C>G	XP_016871921.1:n.51+82C>G
NM_021800.3:c.297+82C>G MANE Select	NP_068572.1:n.297+82C>G
NM_201262.2:c.*55C>G	NP_957714.1:n.*55C>G