Canonical Allele Identifier: CA2668676910
Gene: DNAJC19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180984062G>T , CM000665.2:g.180984062G>T GRCh38
NC_000003.11:g.180701850G>T , CM000665.1:g.180701850G>T GRCh37
NC_000003.10:g.182184544G>T NCBI36
NG_022933.1:g.10713C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000482363.2:n.3042C>A
ENST00000688055.1:c.*1856C>A ENSP00000508688.1:n.*1856C>A
ENST00000382564.8:c.*578C>A MANE Select ENSP00000372005.2:n.*578C>A
ENST00000382564.6:c.*578C>A ENSP00000372005.2:n.*578C>A
ENST00000469657.5:c.*705C>A ENSP00000418058.1:n.*705C>A
NM_001190233.1:c.*578C>A NP_001177162.1:n.*578C>A
NM_145261.3:c.*578C>A NP_660304.1:n.*578C>A
NR_033721.1:n.1049C>A
NR_033722.1:n.1021C>A
NR_033723.1:n.1046C>A
NR_046073.1:n.895C>A
NM_145261.4:c.*578C>A MANE Select NP_660304.1:n.*578C>A
NM_001190233.2:c.*578C>A NP_001177162.1:n.*578C>A
NR_033721.2:n.1011C>A
NR_033722.2:n.983C>A