Canonical Allele Identifier: CA377098512

Gene: DNAJC12

Linked Data

• MyVariant Identifiers: chr10:g.69571274A>C (hg19) ; chr10:g.67811516A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811516A>C , CM000672.2:g.67811516A>C	GRCh38
NC_000010.10:g.69571274A>C , CM000672.1:g.69571274A>C	GRCh37
NC_000010.9:g.69241280A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000225171.7:c.297+8T>G MANE Select	ENSP00000225171.2:n.297+8T>G
ENST00000225171.6:c.297+8T>G	ENSP00000225171.2:n.297+8T>G
ENST00000339758.7:c.305T>G	ENSP00000343575.6:p.Phe102Cys
ENST00000480963.5:c.*217+8T>G	ENSP00000473979.1:n.*217+8T>G
ENST00000483798.6:c.387+8T>G	ENSP00000474215.1:n.387+8T>G
NM_021800.2:c.297+8T>G	NP_068572.1:n.297+8T>G
NM_201262.1:c.305T>G	NP_957714.1:p.Phe102Cys
XM_011539967.1:c.327+8T>G	XP_011538269.1:n.327+8T>G
XM_017016431.1:c.51+8T>G	XP_016871920.1:n.51+8T>G
XM_017016432.2:c.51+8T>G	XP_016871921.1:n.51+8T>G
NM_021800.3:c.297+8T>G MANE Select	NP_068572.1:n.297+8T>G
NM_201262.2:c.305T>G	NP_957714.1:p.Phe102Cys