Canonical Allele Identifier: CA469970085

Gene: DNAJC12

Linked Data

• MyVariant Identifiers: chr10:g.69571366A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811608A>G , CM000672.2:g.67811608A>G	GRCh38
NC_000010.10:g.69571366A>G , CM000672.1:g.69571366A>G	GRCh37
NC_000010.9:g.69241372A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.213T>C MANE Select	ENSP00000225171.2:p.Ser71=
ENST00000225171.6:c.213T>C	ENSP00000225171.2:p.Ser71=
ENST00000339758.7:c.213T>C	ENSP00000343575.6:p.Ser71=
ENST00000480180.1:c.*232T>C	ENSP00000474804.1:n.*232T>C
ENST00000480963.5:c.*133T>C	ENSP00000473979.1:n.*133T>C
ENST00000483798.6:c.303T>C	ENSP00000474215.1:p.Ser101=
NM_021800.2:c.213T>C	NP_068572.1:p.Ser71=
NM_201262.1:c.213T>C	NP_957714.1:p.Ser71=
XM_011539967.1:c.243T>C	XP_011538269.1:p.Ser81=
XM_017016431.1:c.-34T>C	XP_016871920.1:n.-34T>C
XM_017016432.2:c.-34T>C	XP_016871921.1:n.-34T>C
NM_021800.3:c.213T>C MANE Select	NP_068572.1:p.Ser71=
NM_201262.2:c.213T>C	NP_957714.1:p.Ser71=