Canonical Allele Identifier: CA355472538
Gene: DNAJC19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180987005A>T , CM000665.2:g.180987005A>T GRCh38
NC_000003.11:g.180704793A>T , CM000665.1:g.180704793A>T GRCh37
NC_000003.10:g.182187487A>T NCBI36
NG_022933.1:g.7770T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000478723.6:n.218T>A
ENST00000482363.2:n.1314T>A
ENST00000485675.2:n.1308T>A
ENST00000688055.1:c.147T>A ENSP00000508688.1:p.Tyr49Ter
ENST00000382564.8:c.147T>A MANE Select ENSP00000372005.2:p.Tyr49Ter
ENST00000643241.1:c.72T>A ENSP00000496401.1:p.Tyr24Ter
ENST00000646965.1:c.-46-1009T>A ENSP00000496456.1:n.-46-1009T>A
ENST00000382564.6:c.147T>A ENSP00000372005.2:p.Tyr49Ter
ENST00000469657.5:c.130-1009T>A ENSP00000418058.1:n.130-1009T>A
ENST00000478723.5:n.286T>A
ENST00000479269.5:c.72T>A ENSP00000419191.1:p.Tyr24Ter
ENST00000485675.1:n.1220T>A
ENST00000486355.1:c.147T>A ENSP00000419991.1:p.Tyr49Ter
ENST00000491873.5:c.72T>A ENSP00000420767.1:p.Tyr24Ter
NM_001190233.1:c.72T>A NP_001177162.1:p.Tyr24Ter
NM_145261.3:c.147T>A NP_660304.1:p.Tyr49Ter
NR_033721.1:n.267T>A
NR_033722.1:n.302-1009T>A
NR_033723.1:n.319T>A
NR_046073.1:n.176-1009T>A
NM_145261.4:c.147T>A MANE Select NP_660304.1:p.Tyr49Ter
NM_001190233.2:c.72T>A NP_001177162.1:p.Tyr24Ter
NR_033721.2:n.229T>A
NR_033722.2:n.264-1009T>A