Canonical Allele Identifier: CA89106299

Gene: DNAJC19

Linked Data

• dbSNP Id: rs34661228
• MyVariant Identifiers: chr3:g.180701854_180701855insA (hg19) ; chr3:g.180984066_180984067insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180984069dup , CM000665.2:g.180984069dup	GRCh38
NC_000003.11:g.180701857dup , CM000665.1:g.180701857dup	GRCh37
NC_000003.10:g.182184551dup	NCBI36
NG_022933.1:g.10708dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482363.2:n.3037dup
ENST00000688055.1:c.*1851dup	ENSP00000508688.1:n.*1851dup
ENST00000382564.8:c.*573dup MANE Select	ENSP00000372005.2:n.*573dup
ENST00000382564.6:c.*573dup	ENSP00000372005.2:n.*573dup
ENST00000469657.5:c.*700dup	ENSP00000418058.1:n.*700dup
NM_001190233.1:c.*573dup	NP_001177162.1:n.*573dup
NM_145261.3:c.*573dup	NP_660304.1:n.*573dup
NR_033721.1:n.1044dup
NR_033722.1:n.1016dup
NR_033723.1:n.1041dup
NR_046073.1:n.890dup
NM_145261.4:c.*573dup MANE Select	NP_660304.1:n.*573dup
NM_001190233.2:c.*573dup	NP_001177162.1:n.*573dup
NR_033721.2:n.1006dup
NR_033722.2:n.978dup