Canonical Allele Identifier: CA2668676913
Gene: DNAJC19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180984076T>C , CM000665.2:g.180984076T>C GRCh38
NC_000003.11:g.180701864T>C , CM000665.1:g.180701864T>C GRCh37
NC_000003.10:g.182184558T>C NCBI36
NG_022933.1:g.10699A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000482363.2:n.3028A>G
ENST00000688055.1:c.*1842A>G ENSP00000508688.1:n.*1842A>G
ENST00000382564.8:c.*564A>G MANE Select ENSP00000372005.2:n.*564A>G
ENST00000382564.6:c.*564A>G ENSP00000372005.2:n.*564A>G
ENST00000469657.5:c.*691A>G ENSP00000418058.1:n.*691A>G
NM_001190233.1:c.*564A>G NP_001177162.1:n.*564A>G
NM_145261.3:c.*564A>G NP_660304.1:n.*564A>G
NR_033721.1:n.1035A>G
NR_033722.1:n.1007A>G
NR_033723.1:n.1032A>G
NR_046073.1:n.881A>G
NM_145261.4:c.*564A>G MANE Select NP_660304.1:n.*564A>G
NM_001190233.2:c.*564A>G NP_001177162.1:n.*564A>G
NR_033721.2:n.997A>G
NR_033722.2:n.969A>G