Canonical Allele Identifier: CA1057000673
Gene: DNAJC19 HGNC NCBI

Linked Data

dbSNP Id: rs1329229693

Genomic Alleles

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

Transcript Alleles

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