Canonical Allele Identifier: CA2577968112
Gene: DNAJC19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180987048G>T , CM000665.2:g.180987048G>T GRCh38
NC_000003.11:g.180704836G>T , CM000665.1:g.180704836G>T GRCh37
NC_000003.10:g.182187530G>T NCBI36
NG_022933.1:g.7727C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000478723.6:n.201-26C>A
ENST00000482363.2:n.1271C>A
ENST00000485675.2:n.1265C>A
ENST00000688055.1:c.130-26C>A ENSP00000508688.1:n.130-26C>A
ENST00000382564.8:c.130-26C>A MANE Select ENSP00000372005.2:n.130-26C>A
ENST00000643241.1:c.55-26C>A ENSP00000496401.1:n.55-26C>A
ENST00000646965.1:c.-46-1052C>A ENSP00000496456.1:n.-46-1052C>A
ENST00000382564.6:c.130-26C>A ENSP00000372005.2:n.130-26C>A
ENST00000469657.5:c.129+975C>A ENSP00000418058.1:n.129+975C>A
ENST00000478723.5:n.269-26C>A
ENST00000479269.5:c.55-26C>A ENSP00000419191.1:n.55-26C>A
ENST00000485675.1:n.1177C>A
ENST00000486355.1:c.130-26C>A ENSP00000419991.1:n.130-26C>A
ENST00000491873.5:c.55-26C>A ENSP00000420767.1:n.55-26C>A
NM_001190233.1:c.55-26C>A NP_001177162.1:n.55-26C>A
NM_145261.3:c.130-26C>A NP_660304.1:n.130-26C>A
NR_033721.1:n.250-26C>A
NR_033722.1:n.301+975C>A
NR_033723.1:n.302-26C>A
NR_046073.1:n.176-1052C>A
NM_145261.4:c.130-26C>A MANE Select NP_660304.1:n.130-26C>A
NM_001190233.2:c.55-26C>A NP_001177162.1:n.55-26C>A
NR_033721.2:n.212-26C>A
NR_033722.2:n.263+975C>A