Canonical Allele Identifier: CA2668678470
Gene: DNAJC19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180987056_180987057insTTTT , CM000665.2:g.180987056_180987057insTTTT GRCh38
NC_000003.11:g.180704844_180704845insTTTT , CM000665.1:g.180704844_180704845insTTTT GRCh37
NC_000003.10:g.182187538_182187539insTTTT NCBI36
NG_022933.1:g.7718_7719insAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000478723.6:n.201-35_201-34insAAAA
ENST00000482363.2:n.1262_1263insAAAA
ENST00000485675.2:n.1256_1257insAAAA
ENST00000688055.1:c.130-35_130-34insAAAA ENSP00000508688.1:n.130-35_130-34insAAAA
ENST00000382564.8:c.130-35_130-34insAAAA MANE Select ENSP00000372005.2:n.130-35_130-34insAAAA
ENST00000643241.1:c.55-35_55-34insAAAA ENSP00000496401.1:n.55-35_55-34insAAAA
ENST00000646965.1:c.-46-1061_-46-1060insAAAA ENSP00000496456.1:n.-46-1061_-46-1060insAAAA
ENST00000382564.6:c.130-35_130-34insAAAA ENSP00000372005.2:n.130-35_130-34insAAAA
ENST00000469657.5:c.129+966_129+967insAAAA ENSP00000418058.1:n.129+966_129+967insAAAA
ENST00000478723.5:n.269-35_269-34insAAAA
ENST00000479269.5:c.55-35_55-34insAAAA ENSP00000419191.1:n.55-35_55-34insAAAA
ENST00000485675.1:n.1168_1169insAAAA
ENST00000486355.1:c.130-35_130-34insAAAA ENSP00000419991.1:n.130-35_130-34insAAAA
ENST00000491873.5:c.55-35_55-34insAAAA ENSP00000420767.1:n.55-35_55-34insAAAA
NM_001190233.1:c.55-35_55-34insAAAA NP_001177162.1:n.55-35_55-34insAAAA
NM_145261.3:c.130-35_130-34insAAAA NP_660304.1:n.130-35_130-34insAAAA
NR_033721.1:n.250-35_250-34insAAAA
NR_033722.1:n.301+966_301+967insAAAA
NR_033723.1:n.302-35_302-34insAAAA
NR_046073.1:n.176-1061_176-1060insAAAA
NM_145261.4:c.130-35_130-34insAAAA MANE Select NP_660304.1:n.130-35_130-34insAAAA
NM_001190233.2:c.55-35_55-34insAAAA NP_001177162.1:n.55-35_55-34insAAAA
NR_033721.2:n.212-35_212-34insAAAA
NR_033722.2:n.263+966_263+967insAAAA