Canonical Allele Identifier: CA2759631443
Gene: DNAJC19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180988143_180988144del , CM000665.2:g.180988143_180988144del GRCh38
NC_000003.11:g.180705931_180705932del , CM000665.1:g.180705931_180705932del GRCh37
NC_000003.10:g.182188625_182188626del NCBI36
NG_022933.1:g.6633_6634del

Transcript Alleles

HGVS Amino-acid Change
ENST00000478723.6:n.126+36_126+37del
ENST00000482363.2:n.222+36_222+37del
ENST00000485675.2:n.216+36_216+37del
ENST00000688055.1:c.55+36_55+37del ENSP00000508688.1:n.55+36_55+37del
ENST00000382564.8:c.55+36_55+37del MANE Select ENSP00000372005.2:n.55+36_55+37del
ENST00000643241.1:c.-21+36_-21+37del ENSP00000496401.1:n.-21+36_-21+37del
ENST00000646965.1:c.-47+1458_-47+1459del ENSP00000496456.1:n.-47+1458_-47+1459del
ENST00000382564.6:c.55+36_55+37del ENSP00000372005.2:n.55+36_55+37del
ENST00000469657.5:c.55+36_55+37del ENSP00000418058.1:n.55+36_55+37del
ENST00000472504.1:n.263_264del
ENST00000478723.5:n.194+36_194+37del
ENST00000479269.5:c.-21+36_-21+37del ENSP00000419191.1:n.-21+36_-21+37del
ENST00000482363.1:n.216+36_216+37del
ENST00000485675.1:n.129-46_129-45del
ENST00000486355.1:c.55+36_55+37del ENSP00000419991.1:n.55+36_55+37del
ENST00000491873.5:c.-20-46_-20-45del ENSP00000420767.1:n.-20-46_-20-45del
NM_001190233.1:c.-21+36_-21+37del NP_001177162.1:n.-21+36_-21+37del
NM_145261.3:c.55+36_55+37del NP_660304.1:n.55+36_55+37del
NR_033721.1:n.176-46_176-45del
NR_033722.1:n.227+36_227+37del
NR_033723.1:n.227+36_227+37del
NR_046073.1:n.175+1458_175+1459del
NM_145261.4:c.55+36_55+37del MANE Select NP_660304.1:n.55+36_55+37del
NM_001190233.2:c.-21+36_-21+37del NP_001177162.1:n.-21+36_-21+37del
NR_033721.2:n.138-46_138-45del
NR_033722.2:n.189+36_189+37del