Canonical Allele Identifier: CA2606706147

Gene: DNAJC19

Linked Data

• gnomAD v3: 3-180984049-TACTATTTTTAATGCATGAA-T
• gnomAD v4: 3-180984049-TACTATTTTTAATGCATGAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180984051_180984069del , CM000665.2:g.180984051_180984069del	GRCh38
NC_000003.11:g.180701839_180701857del , CM000665.1:g.180701839_180701857del	GRCh37
NC_000003.10:g.182184533_182184551del	NCBI36
NG_022933.1:g.10707_10725del

Transcript Alleles

HGVS	Amino-acid change
ENST00000482363.2:n.3036_3054del
ENST00000688055.1:c.*1850_*1868del	ENSP00000508688.1:n.*1850_*1868del
ENST00000382564.8:c.*572_*590del MANE Select	ENSP00000372005.2:n.*572_*590del
ENST00000382564.6:c.*572_*590del	ENSP00000372005.2:n.*572_*590del
ENST00000469657.5:c.*699_*717del	ENSP00000418058.1:n.*699_*717del
NM_001190233.1:c.*572_*590del	NP_001177162.1:n.*572_*590del
NM_145261.3:c.*572_*590del	NP_660304.1:n.*572_*590del
NR_033721.1:n.1043_1061del
NR_033722.1:n.1015_1033del
NR_033723.1:n.1040_1058del
NR_046073.1:n.889_907del
NM_145261.4:c.*572_*590del MANE Select	NP_660304.1:n.*572_*590del
NM_001190233.2:c.*572_*590del	NP_001177162.1:n.*572_*590del
NR_033721.2:n.1005_1023del
NR_033722.2:n.977_995del