Canonical Allele Identifier: CA377098677

Gene: DNAJC12

Linked Data

• MyVariant Identifiers: chr10:g.69571347A>G (hg19) ; chr10:g.67811589A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811589A>G , CM000672.2:g.67811589A>G	GRCh38
NC_000010.10:g.69571347A>G , CM000672.1:g.69571347A>G	GRCh37
NC_000010.9:g.69241353A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.232T>C MANE Select	ENSP00000225171.2:p.Trp78Arg
ENST00000225171.6:c.232T>C	ENSP00000225171.2:p.Trp78Arg
ENST00000339758.7:c.232T>C	ENSP00000343575.6:p.Trp78Arg
ENST00000480180.1:c.*251T>C	ENSP00000474804.1:n.*251T>C
ENST00000480963.5:c.*152T>C	ENSP00000473979.1:n.*152T>C
ENST00000483798.6:c.322T>C	ENSP00000474215.1:p.Trp108Arg
NM_021800.2:c.232T>C	NP_068572.1:p.Trp78Arg
NM_201262.1:c.232T>C	NP_957714.1:p.Trp78Arg
XM_011539967.1:c.262T>C	XP_011538269.1:p.Trp88Arg
XM_017016431.1:c.-15T>C	XP_016871920.1:n.-15T>C
XM_017016432.2:c.-15T>C	XP_016871921.1:n.-15T>C
NM_021800.3:c.232T>C MANE Select	NP_068572.1:p.Trp78Arg
NM_201262.2:c.232T>C	NP_957714.1:p.Trp78Arg