Canonical Allele Identifier: CA89106660
Gene: DNAJC19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180988022C>T , CM000665.2:g.180988022C>T GRCh38
NC_000003.11:g.180705810C>T , CM000665.1:g.180705810C>T GRCh37
NC_000003.10:g.182188504C>T NCBI36
NG_022933.1:g.6753G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000478723.6:n.200+1G>A
ENST00000482363.2:n.297G>A
ENST00000485675.2:n.291G>A
ENST00000688055.1:c.129+1G>A ENSP00000508688.1:n.129+1G>A
ENST00000382564.8:c.129+1G>A MANE Select ENSP00000372005.2:n.129+1G>A
ENST00000643241.1:c.54+1G>A ENSP00000496401.1:n.54+1G>A
ENST00000646965.1:c.-47+1578G>A ENSP00000496456.1:n.-47+1578G>A
ENST00000382564.6:c.129+1G>A ENSP00000372005.2:n.129+1G>A
ENST00000469657.5:c.129+1G>A ENSP00000418058.1:n.129+1G>A
ENST00000472504.1:n.383G>A
ENST00000478723.5:n.268+1G>A
ENST00000479269.5:c.54+1G>A ENSP00000419191.1:n.54+1G>A
ENST00000482363.1:n.291G>A
ENST00000485675.1:n.203G>A
ENST00000486355.1:c.129+1G>A ENSP00000419991.1:n.129+1G>A
ENST00000491873.5:c.54+1G>A ENSP00000420767.1:n.54+1G>A
NM_001190233.1:c.54+1G>A NP_001177162.1:n.54+1G>A
NM_145261.3:c.129+1G>A NP_660304.1:n.129+1G>A
NR_033721.1:n.249+1G>A
NR_033722.1:n.301+1G>A
NR_033723.1:n.301+1G>A
NR_046073.1:n.175+1578G>A
NM_145261.4:c.129+1G>A MANE Select NP_660304.1:n.129+1G>A
NM_001190233.2:c.54+1G>A NP_001177162.1:n.54+1G>A
NR_033721.2:n.211+1G>A
NR_033722.2:n.263+1G>A