Canonical Allele Identifier: CA2609360317

Gene: DNAJC12

Linked Data

• gnomAD v4: 10-67811402-CTCTGCTAACTTCTTGGTTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67811406_67811424del , CM000672.2:g.67811406_67811424del	GRCh38
NC_000010.10:g.69571164_69571182del , CM000672.1:g.69571164_69571182del	GRCh37
NC_000010.9:g.69241170_69241188del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225171.7:c.297+103_297+121del MANE Select	ENSP00000225171.2:n.297+103_297+121del
ENST00000225171.6:c.297+103_297+121del	ENSP00000225171.2:n.297+103_297+121del
ENST00000339758.7:c.*76_*94del	ENSP00000343575.6:n.*76_*94del
ENST00000480963.5:c.*217+103_*217+121del	ENSP00000473979.1:n.*217+103_*217+121del
ENST00000483798.6:c.387+103_387+121del	ENSP00000474215.1:n.387+103_387+121del
NM_021800.2:c.297+103_297+121del	NP_068572.1:n.297+103_297+121del
NM_201262.1:c.*76_*94del	NP_957714.1:n.*76_*94del
XM_011539967.1:c.327+103_327+121del	XP_011538269.1:n.327+103_327+121del
XM_017016431.1:c.51+103_51+121del	XP_016871920.1:n.51+103_51+121del
XM_017016432.2:c.51+103_51+121del	XP_016871921.1:n.51+103_51+121del
NM_021800.3:c.297+103_297+121del MANE Select	NP_068572.1:n.297+103_297+121del
NM_201262.2:c.*76_*94del	NP_957714.1:n.*76_*94del