Canonical Allele Identifier: CA1424458963
Gene: DNAJC19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180984085T= , CM000665.2:g.180984085T= GRCh38
NC_000003.11:g.180701873T= , CM000665.1:g.180701873T= GRCh37
NC_000003.10:g.182184567T= NCBI36
NG_022933.1:g.10690A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000482363.2:n.3019A=
ENST00000688055.1:c.*1833A= ENSP00000508688.1:n.*1833A=
ENST00000382564.8:c.*555A= MANE Select ENSP00000372005.2:n.*555A=
ENST00000382564.6:c.*555A= ENSP00000372005.2:n.*555A=
ENST00000469657.5:c.*682A= ENSP00000418058.1:n.*682A=
NM_001190233.1:c.*555A= NP_001177162.1:n.*555A=
NM_145261.3:c.*555A= NP_660304.1:n.*555A=
NR_033721.1:n.1026A=
NR_033722.1:n.998A=
NR_033723.1:n.1023A=
NR_046073.1:n.872A=
NM_145261.4:c.*555A= MANE Select NP_660304.1:n.*555A=
NM_001190233.2:c.*555A= NP_001177162.1:n.*555A=
NR_033721.2:n.988A=
NR_033722.2:n.960A=