Canonical Allele Identifier: CA2572185726

Gene: DNAJC19

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180986988_180986989del , CM000665.2:g.180986988_180986989del	GRCh38
NC_000003.11:g.180704776_180704777del , CM000665.1:g.180704776_180704777del	GRCh37
NC_000003.10:g.182187470_182187471del	NCBI36
NG_022933.1:g.7786_7787del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.234_235del
ENST00000482363.2:n.1330_1331del
ENST00000485675.2:n.1324_1325del
ENST00000688055.1:c.163_164del	ENSP00000508688.1:p.Glu55ThrfsTer20
ENST00000382564.8:c.163_164del MANE Select	ENSP00000372005.2:p.Glu55ThrfsTer20
ENST00000643241.1:c.88_89del	ENSP00000496401.1:p.Glu30ThrfsTer22
ENST00000646965.1:c.-46-993_-46-992del	ENSP00000496456.1:n.-46-993_-46-992del
ENST00000382564.6:c.163_164del	ENSP00000372005.2:p.Glu55ThrfsTer20
ENST00000469657.5:c.130-993_130-992del	ENSP00000418058.1:n.130-993_130-992del
ENST00000478723.5:n.302_303del
ENST00000479269.5:c.88_89del	ENSP00000419191.1:p.Glu30ThrfsTer20
ENST00000485675.1:n.1236_1237del
ENST00000486355.1:c.154+9_154+10del	ENSP00000419991.1:n.154+9_154+10del
ENST00000491873.5:c.88_89del	ENSP00000420767.1:p.Glu30ThrfsTer20
NM_001190233.1:c.88_89del	NP_001177162.1:p.Glu30ThrfsTer20
NM_145261.3:c.163_164del	NP_660304.1:p.Glu55ThrfsTer20
NR_033721.1:n.283_284del
NR_033722.1:n.302-993_302-992del
NR_033723.1:n.326+9_326+10del
NR_046073.1:n.176-993_176-992del
NM_145261.4:c.163_164del MANE Select	NP_660304.1:p.Glu55ThrfsTer20
NM_001190233.2:c.88_89del	NP_001177162.1:p.Glu30ThrfsTer20
NR_033721.2:n.245_246del
NR_033722.2:n.264-993_264-992del