Canonical Allele Identifier: CA377098676

Gene: DNAJC12

Linked Data

• COSMIC: COSM4015200 ; COSM4015201
• MyVariant Identifiers: chr10:g.69571347A>C (hg19) ; chr10:g.67811589A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.232T>G MANE Select	ENSP00000225171.2:p.Trp78Gly
ENST00000225171.6:c.232T>G	ENSP00000225171.2:p.Trp78Gly
ENST00000339758.7:c.232T>G	ENSP00000343575.6:p.Trp78Gly
ENST00000480180.1:c.*251T>G	ENSP00000474804.1:n.*251T>G
ENST00000480963.5:c.*152T>G	ENSP00000473979.1:n.*152T>G
ENST00000483798.6:c.322T>G	ENSP00000474215.1:p.Trp108Gly
NM_021800.2:c.232T>G	NP_068572.1:p.Trp78Gly
NM_201262.1:c.232T>G	NP_957714.1:p.Trp78Gly
XM_011539967.1:c.262T>G	XP_011538269.1:p.Trp88Gly
XM_017016431.1:c.-15T>G	XP_016871920.1:n.-15T>G
XM_017016432.2:c.-15T>G	XP_016871921.1:n.-15T>G
NM_021800.3:c.232T>G MANE Select	NP_068572.1:p.Trp78Gly
NM_201262.2:c.232T>G	NP_957714.1:p.Trp78Gly