Canonical Allele Identifier: CA377098651

Gene: DNAJC12

Linked Data

• MyVariant Identifiers: chr10:g.69571335G>C (hg19) ; chr10:g.67811577G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811577G>C , CM000672.2:g.67811577G>C	GRCh38
NC_000010.10:g.69571335G>C , CM000672.1:g.69571335G>C	GRCh37
NC_000010.9:g.69241341G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.244C>G MANE Select	ENSP00000225171.2:p.Gln82Glu
ENST00000225171.6:c.244C>G	ENSP00000225171.2:p.Gln82Glu
ENST00000339758.7:c.244C>G	ENSP00000343575.6:p.Gln82Glu
ENST00000480180.1:c.*263C>G	ENSP00000474804.1:n.*263C>G
ENST00000480963.5:c.*164C>G	ENSP00000473979.1:n.*164C>G
ENST00000483798.6:c.334C>G	ENSP00000474215.1:p.Gln112Glu
NM_021800.2:c.244C>G	NP_068572.1:p.Gln82Glu
NM_201262.1:c.244C>G	NP_957714.1:p.Gln82Glu
XM_011539967.1:c.274C>G	XP_011538269.1:p.Gln92Glu
XM_017016431.1:c.-3C>G	XP_016871920.1:n.-3C>G
XM_017016432.2:c.-3C>G	XP_016871921.1:n.-3C>G
NM_021800.3:c.244C>G MANE Select	NP_068572.1:p.Gln82Glu
NM_201262.2:c.244C>G	NP_957714.1:p.Gln82Glu