Canonical Allele Identifier: CA469970079

Gene: DNAJC12

Linked Data

• MyVariant Identifiers: chr10:g.69571363T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811605T>G , CM000672.2:g.67811605T>G	GRCh38
NC_000010.10:g.69571363T>G , CM000672.1:g.69571363T>G	GRCh37
NC_000010.9:g.69241369T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.216A>C MANE Select	ENSP00000225171.2:p.Arg72=
ENST00000225171.6:c.216A>C	ENSP00000225171.2:p.Arg72=
ENST00000339758.7:c.216A>C	ENSP00000343575.6:p.Arg72=
ENST00000480180.1:c.*235A>C	ENSP00000474804.1:n.*235A>C
ENST00000480963.5:c.*136A>C	ENSP00000473979.1:n.*136A>C
ENST00000483798.6:c.306A>C	ENSP00000474215.1:p.Arg102=
NM_021800.2:c.216A>C	NP_068572.1:p.Arg72=
NM_201262.1:c.216A>C	NP_957714.1:p.Arg72=
XM_011539967.1:c.246A>C	XP_011538269.1:p.Arg82=
XM_017016431.1:c.-31A>C	XP_016871920.1:n.-31A>C
XM_017016432.2:c.-31A>C	XP_016871921.1:n.-31A>C
NM_021800.3:c.216A>C MANE Select	NP_068572.1:p.Arg72=
NM_201262.2:c.216A>C	NP_957714.1:p.Arg72=