Canonical Allele Identifier: CA377098685

Gene: DNAJC12

Linked Data

• MyVariant Identifiers: chr10:g.69571350G>C (hg19) ; chr10:g.67811592G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811592G>C , CM000672.2:g.67811592G>C	GRCh38
NC_000010.10:g.69571350G>C , CM000672.1:g.69571350G>C	GRCh37
NC_000010.9:g.69241356G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.229C>G MANE Select	ENSP00000225171.2:p.His77Asp
ENST00000225171.6:c.229C>G	ENSP00000225171.2:p.His77Asp
ENST00000339758.7:c.229C>G	ENSP00000343575.6:p.His77Asp
ENST00000480180.1:c.*248C>G	ENSP00000474804.1:n.*248C>G
ENST00000480963.5:c.*149C>G	ENSP00000473979.1:n.*149C>G
ENST00000483798.6:c.319C>G	ENSP00000474215.1:p.His107Asp
NM_021800.2:c.229C>G	NP_068572.1:p.His77Asp
NM_201262.1:c.229C>G	NP_957714.1:p.His77Asp
XM_011539967.1:c.259C>G	XP_011538269.1:p.His87Asp
XM_017016431.1:c.-18C>G	XP_016871920.1:n.-18C>G
XM_017016432.2:c.-18C>G	XP_016871921.1:n.-18C>G
NM_021800.3:c.229C>G MANE Select	NP_068572.1:p.His77Asp
NM_201262.2:c.229C>G	NP_957714.1:p.His77Asp