Canonical Allele Identifier: CA548508104

Gene: DNAJC19

Linked Data

• dbSNP Id: rs1560037497
• gnomAD v2: 3-180701849-T-TGAAATACTATTTATTTTAGCATGAAATAAAATTTTAGCATGAAATATATATTTTAGCATGAAATAATATTTTA
• gnomAD v4: 3-180984061-T-TGAAATACTATTTATTTTAGCATGAAATAAAATTTTAGCATGAAATATATATTTTAGCATGAAATAATATTTTA
• MyVariant Identifiers: chr3:g.180701849_180701850insGAAATACTATTTATTTTAGCATGAAATAAAATTTTAGCATGAAATATATATTTTAGCATGAAATAATATTTTA (hg19) ; chr3:g.180984061_180984062insGAAATACTATTTATTTTAGCATGAAATAAAATTTTAGCATGAAATATATATTTTAGCATGAAATAATATTTTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180984062_180984063insAAATACTATTTATTTTAGCATGAAATAAAATTTTAGCATGAAATATATATTTTAGCATGAAATAATATTTTAG , CM000665.2:g.180984062_180984063insAAATACTATTTATTTTAGCATGAAATAAAATTTTAGCATGAAATATATATTTTAGCATGAAATAATATTTTAG	GRCh38
NC_000003.11:g.180701850_180701851insAAATACTATTTATTTTAGCATGAAATAAAATTTTAGCATGAAATATATATTTTAGCATGAAATAATATTTTAG , CM000665.1:g.180701850_180701851insAAATACTATTTATTTTAGCATGAAATAAAATTTTAGCATGAAATATATATTTTAGCATGAAATAATATTTTAG	GRCh37
NC_000003.10:g.182184544_182184545insAAATACTATTTATTTTAGCATGAAATAAAATTTTAGCATGAAATATATATTTTAGCATGAAATAATATTTTAG	NCBI36
NG_022933.1:g.10713_10714insTAAAATATTATTTCATGCTAAAATATATATTTCATGCTAAAATTTTATTTCATGCTAAAATAAATAGTATTTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000482363.2:n.3042_3043insTAAAATATTATTTCATGCTAAAATATATATTTCATGCTAAAATTTTATTTCATGCTAAAATAAATAGTATTTC
ENST00000688055.1:c.*1856_*1857insTAAAATATTATTTCATGCTAAAATATATATTTCATGCTAAAATTTTATTTCATGCTAAAATAAATAGTATTTC	ENSP00000508688.1:n.*1856_*1857insTAAAATATTATTTCATGCTAAAATATA...
ENST00000382564.8:c.*578_*579insTAAAATATTATTTCATGCTAAAATATATATTTCATGCTAAAATTTTATTTCATGCTAAAATAAATAGTATTTC MANE Select	ENSP00000372005.2:n.*578_*579insTAAAATATTATTTCATGCTAAAATATATA...
ENST00000382564.6:c.*578_*579insTAAAATATTATTTCATGCTAAAATATATATTTCATGCTAAAATTTTATTTCATGCTAAAATAAATAGTATTTC	ENSP00000372005.2:n.*578_*579insTAAAATATTATTTCATGCTAAAATATATA...
ENST00000469657.5:c.*705_*706insTAAAATATTATTTCATGCTAAAATATATATTTCATGCTAAAATTTTATTTCATGCTAAAATAAATAGTATTTC	ENSP00000418058.1:n.*705_*706insTAAAATATTATTTCATGCTAAAATATATA...
NM_001190233.1:c.*578_*579insTAAAATATTATTTCATGCTAAAATATATATTTCATGCTAAAATTTTATTTCATGCTAAAATAAATAGTATTTC	NP_001177162.1:n.*578_*579insTAAAATATTATTTCATGCTAAAATATATATTT...
NM_145261.3:c.*578_*579insTAAAATATTATTTCATGCTAAAATATATATTTCATGCTAAAATTTTATTTCATGCTAAAATAAATAGTATTTC	NP_660304.1:n.*578_*579insTAAAATATTATTTCATGCTAAAATATATATTTCAT...
NR_033721.1:n.1049_1050insTAAAATATTATTTCATGCTAAAATATATATTTCATGCTAAAATTTTATTTCATGCTAAAATAAATAGTATTTC
NR_033722.1:n.1021_1022insTAAAATATTATTTCATGCTAAAATATATATTTCATGCTAAAATTTTATTTCATGCTAAAATAAATAGTATTTC
NR_033723.1:n.1046_1047insTAAAATATTATTTCATGCTAAAATATATATTTCATGCTAAAATTTTATTTCATGCTAAAATAAATAGTATTTC
NR_046073.1:n.895_896insTAAAATATTATTTCATGCTAAAATATATATTTCATGCTAAAATTTTATTTCATGCTAAAATAAATAGTATTTC
NM_145261.4:c.*578_*579insTAAAATATTATTTCATGCTAAAATATATATTTCATGCTAAAATTTTATTTCATGCTAAAATAAATAGTATTTC MANE Select	NP_660304.1:n.*578_*579insTAAAATATTATTTCATGCTAAAATATATATTTCAT...
NM_001190233.2:c.*578_*579insTAAAATATTATTTCATGCTAAAATATATATTTCATGCTAAAATTTTATTTCATGCTAAAATAAATAGTATTTC	NP_001177162.1:n.*578_*579insTAAAATATTATTTCATGCTAAAATATATATTT...
NR_033721.2:n.1011_1012insTAAAATATTATTTCATGCTAAAATATATATTTCATGCTAAAATTTTATTTCATGCTAAAATAAATAGTATTTC
NR_033722.2:n.983_984insTAAAATATTATTTCATGCTAAAATATATATTTCATGCTAAAATTTTATTTCATGCTAAAATAAATAGTATTTC