Canonical Allele Identifier: CA2704719808
Gene: DNAJC19 HGNC NCBI

Linked Data

dbSNP Id: rs145145539

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180987062_180987066dup , CM000665.2:g.180987062_180987066dup GRCh38
NC_000003.11:g.180704850_180704854dup , CM000665.1:g.180704850_180704854dup GRCh37
NC_000003.10:g.182187544_182187548dup NCBI36
NG_022933.1:g.7715_7719dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000478723.6:n.201-38_201-34dup
ENST00000482363.2:n.1259_1263dup
ENST00000485675.2:n.1253_1257dup
ENST00000688055.1:c.130-38_130-34dup ENSP00000508688.1:n.130-38_130-34dup
ENST00000382564.8:c.130-38_130-34dup MANE Select ENSP00000372005.2:n.130-38_130-34dup
ENST00000643241.1:c.55-38_55-34dup ENSP00000496401.1:n.55-38_55-34dup
ENST00000646965.1:c.-46-1064_-46-1060dup ENSP00000496456.1:n.-46-1064_-46-1060dup
ENST00000382564.6:c.130-38_130-34dup ENSP00000372005.2:n.130-38_130-34dup
ENST00000469657.5:c.129+963_129+967dup ENSP00000418058.1:n.129+963_129+967dup
ENST00000478723.5:n.269-38_269-34dup
ENST00000479269.5:c.55-38_55-34dup ENSP00000419191.1:n.55-38_55-34dup
ENST00000485675.1:n.1165_1169dup
ENST00000486355.1:c.130-38_130-34dup ENSP00000419991.1:n.130-38_130-34dup
ENST00000491873.5:c.55-38_55-34dup ENSP00000420767.1:n.55-38_55-34dup
NM_001190233.1:c.55-38_55-34dup NP_001177162.1:n.55-38_55-34dup
NM_145261.3:c.130-38_130-34dup NP_660304.1:n.130-38_130-34dup
NR_033721.1:n.250-38_250-34dup
NR_033722.1:n.301+963_301+967dup
NR_033723.1:n.302-38_302-34dup
NR_046073.1:n.176-1064_176-1060dup
NM_145261.4:c.130-38_130-34dup MANE Select NP_660304.1:n.130-38_130-34dup
NM_001190233.2:c.55-38_55-34dup NP_001177162.1:n.55-38_55-34dup
NR_033721.2:n.212-38_212-34dup
NR_033722.2:n.263+963_263+967dup