Canonical Allele Identifier: CA377098627

Gene: DNAJC12

Linked Data

• MyVariant Identifiers: chr10:g.69571325A>C (hg19) ; chr10:g.67811567A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811567A>C , CM000672.2:g.67811567A>C	GRCh38
NC_000010.10:g.69571325A>C , CM000672.1:g.69571325A>C	GRCh37
NC_000010.9:g.69241331A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.254T>G MANE Select	ENSP00000225171.2:p.Met85Arg
ENST00000225171.6:c.254T>G	ENSP00000225171.2:p.Met85Arg
ENST00000339758.7:c.254T>G	ENSP00000343575.6:p.Met85Arg
ENST00000480180.1:c.*273T>G	ENSP00000474804.1:n.*273T>G
ENST00000480963.5:c.*174T>G	ENSP00000473979.1:n.*174T>G
ENST00000483798.6:c.344T>G	ENSP00000474215.1:p.Met115Arg
NM_021800.2:c.254T>G	NP_068572.1:p.Met85Arg
NM_201262.1:c.254T>G	NP_957714.1:p.Met85Arg
XM_011539967.1:c.284T>G	XP_011538269.1:p.Met95Arg
XM_017016431.1:c.8T>G	XP_016871920.1:p.Met3Arg
XM_017016432.2:c.8T>G	XP_016871921.1:p.Met3Arg
NM_021800.3:c.254T>G MANE Select	NP_068572.1:p.Met85Arg
NM_201262.2:c.254T>G	NP_957714.1:p.Met85Arg