Canonical Allele Identifier: CA548508115

Gene: DNAJC19

Linked Data

• dbSNP Id: rs1560037525
• gnomAD v2: 3-180701884-T-C
• gnomAD v3: 3-180984096-T-C
• gnomAD v4: 3-180984096-T-C
• MyVariant Identifiers: chr3:g.180701884_180701886delinsCAC (hg19) ; chr3:g.180701884_180701888delinsCACAC (hg19) ; chr3:g.180984096_180984098delinsCAC (hg38) ; chr3:g.180984096_180984100delinsCACAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180984096T>C , CM000665.2:g.180984096T>C	GRCh38
NC_000003.11:g.180701884T>C , CM000665.1:g.180701884T>C	GRCh37
NC_000003.10:g.182184578T>C	NCBI36
NG_022933.1:g.10679A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000482363.2:n.3008A>G
ENST00000688055.1:c.*1822A>G	ENSP00000508688.1:n.*1822A>G
ENST00000382564.8:c.*544A>G MANE Select	ENSP00000372005.2:n.*544A>G
ENST00000382564.6:c.*544A>G	ENSP00000372005.2:n.*544A>G
ENST00000469657.5:c.*671A>G	ENSP00000418058.1:n.*671A>G
NM_001190233.1:c.*544A>G	NP_001177162.1:n.*544A>G
NM_145261.3:c.*544A>G	NP_660304.1:n.*544A>G
NR_033721.1:n.1015A>G
NR_033722.1:n.987A>G
NR_033723.1:n.1012A>G
NR_046073.1:n.861A>G
NM_145261.4:c.*544A>G MANE Select	NP_660304.1:n.*544A>G
NM_001190233.2:c.*544A>G	NP_001177162.1:n.*544A>G
NR_033721.2:n.977A>G
NR_033722.2:n.949A>G