Canonical Allele Identifier: CA2609360333

Gene: DNAJC12

Linked Data

• gnomAD v4: 10-67811445-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811445T>G , CM000672.2:g.67811445T>G	GRCh38
NC_000010.10:g.69571203T>G , CM000672.1:g.69571203T>G	GRCh37
NC_000010.9:g.69241209T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.297+79A>C MANE Select	ENSP00000225171.2:n.297+79A>C
ENST00000225171.6:c.297+79A>C	ENSP00000225171.2:n.297+79A>C
ENST00000339758.7:c.*52A>C	ENSP00000343575.6:n.*52A>C
ENST00000480963.5:c.*217+79A>C	ENSP00000473979.1:n.*217+79A>C
ENST00000483798.6:c.387+79A>C	ENSP00000474215.1:n.387+79A>C
NM_021800.2:c.297+79A>C	NP_068572.1:n.297+79A>C
NM_201262.1:c.*52A>C	NP_957714.1:n.*52A>C
XM_011539967.1:c.327+79A>C	XP_011538269.1:n.327+79A>C
XM_017016431.1:c.51+79A>C	XP_016871920.1:n.51+79A>C
XM_017016432.2:c.51+79A>C	XP_016871921.1:n.51+79A>C
NM_021800.3:c.297+79A>C MANE Select	NP_068572.1:n.297+79A>C
NM_201262.2:c.*52A>C	NP_957714.1:n.*52A>C