Canonical Allele Identifier: CA548508102

Gene: DNAJC19

Linked Data

• dbSNP Id: rs1305678900
• gnomAD v2: 3-180701847-A-AGT
• gnomAD v4: 3-180984059-A-AGT
• MyVariant Identifiers: chr3:g.180701847_180701848insGT (hg19) ; chr3:g.180984059_180984060insGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180984059_180984060insGT , CM000665.2:g.180984059_180984060insGT	GRCh38
NC_000003.11:g.180701847_180701848insGT , CM000665.1:g.180701847_180701848insGT	GRCh37
NC_000003.10:g.182184541_182184542insGT	NCBI36
NG_022933.1:g.10715_10716insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482363.2:n.3044_3045insAC
ENST00000688055.1:c.*1858_*1859insAC	ENSP00000508688.1:n.*1858_*1859insAC
ENST00000382564.8:c.*580_*581insAC MANE Select	ENSP00000372005.2:n.*580_*581insAC
ENST00000382564.6:c.*580_*581insAC	ENSP00000372005.2:n.*580_*581insAC
ENST00000469657.5:c.*707_*708insAC	ENSP00000418058.1:n.*707_*708insAC
NM_001190233.1:c.*580_*581insAC	NP_001177162.1:n.*580_*581insAC
NM_145261.3:c.*580_*581insAC	NP_660304.1:n.*580_*581insAC
NR_033721.1:n.1051_1052insAC
NR_033722.1:n.1023_1024insAC
NR_033723.1:n.1048_1049insAC
NR_046073.1:n.897_898insAC
NM_145261.4:c.*580_*581insAC MANE Select	NP_660304.1:n.*580_*581insAC
NM_001190233.2:c.*580_*581insAC	NP_001177162.1:n.*580_*581insAC
NR_033721.2:n.1013_1014insAC
NR_033722.2:n.985_986insAC