Canonical Allele Identifier: CA377098599

Gene: DNAJC12

Linked Data

• MyVariant Identifiers: chr10:g.69571314G>A (hg19) ; chr10:g.67811556G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811556G>A , CM000672.2:g.67811556G>A	GRCh38
NC_000010.10:g.69571314G>A , CM000672.1:g.69571314G>A	GRCh37
NC_000010.9:g.69241320G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.265C>T MANE Select	ENSP00000225171.2:p.Gln89Ter
ENST00000225171.6:c.265C>T	ENSP00000225171.2:p.Gln89Ter
ENST00000339758.7:c.265C>T	ENSP00000343575.6:p.Gln89Ter
ENST00000480180.1:c.*284C>T	ENSP00000474804.1:n.*284C>T
ENST00000480963.5:c.*185C>T	ENSP00000473979.1:n.*185C>T
ENST00000483798.6:c.355C>T	ENSP00000474215.1:p.Gln119Ter
NM_021800.2:c.265C>T	NP_068572.1:p.Gln89Ter
NM_201262.1:c.265C>T	NP_957714.1:p.Gln89Ter
XM_011539967.1:c.295C>T	XP_011538269.1:p.Gln99Ter
XM_017016431.1:c.19C>T	XP_016871920.1:p.Gln7Ter
XM_017016432.2:c.19C>T	XP_016871921.1:p.Gln7Ter
NM_021800.3:c.265C>T MANE Select	NP_068572.1:p.Gln89Ter
NM_201262.2:c.265C>T	NP_957714.1:p.Gln89Ter