Canonical Allele Identifier: CA469970072

Gene: DNAJC12

Linked Data

• dbSNP Id: rs1182475977
• gnomAD v2: 10-69571357-G-A
• gnomAD v4: 10-67811599-G-A
• MyVariant Identifiers: chr10:g.69571357G>A (hg19) ; chr10:g.67811599G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811599G>A , CM000672.2:g.67811599G>A	GRCh38
NC_000010.10:g.69571357G>A , CM000672.1:g.69571357G>A	GRCh37
NC_000010.9:g.69241363G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.222C>T MANE Select	ENSP00000225171.2:p.Arg74=
ENST00000225171.6:c.222C>T	ENSP00000225171.2:p.Arg74=
ENST00000339758.7:c.222C>T	ENSP00000343575.6:p.Arg74=
ENST00000480180.1:c.*241C>T	ENSP00000474804.1:n.*241C>T
ENST00000480963.5:c.*142C>T	ENSP00000473979.1:n.*142C>T
ENST00000483798.6:c.312C>T	ENSP00000474215.1:p.Arg104=
NM_021800.2:c.222C>T	NP_068572.1:p.Arg74=
NM_201262.1:c.222C>T	NP_957714.1:p.Arg74=
XM_011539967.1:c.252C>T	XP_011538269.1:p.Arg84=
XM_017016431.1:c.-25C>T	XP_016871920.1:n.-25C>T
XM_017016432.2:c.-25C>T	XP_016871921.1:n.-25C>T
NM_021800.3:c.222C>T MANE Select	NP_068572.1:p.Arg74=
NM_201262.2:c.222C>T	NP_957714.1:p.Arg74=