Canonical Allele Identifier: CA1057002256
Gene: DNAJC19 HGNC NCBI

Linked Data

dbSNP Id: rs1715005436

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180988143C>T , CM000665.2:g.180988143C>T GRCh38
NC_000003.11:g.180705931C>T , CM000665.1:g.180705931C>T GRCh37
NC_000003.10:g.182188625C>T NCBI36
NG_022933.1:g.6632G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000478723.6:n.126+35G>A
ENST00000482363.2:n.222+35G>A
ENST00000485675.2:n.216+35G>A
ENST00000688055.1:c.55+35G>A ENSP00000508688.1:n.55+35G>A
ENST00000382564.8:c.55+35G>A MANE Select ENSP00000372005.2:n.55+35G>A
ENST00000643241.1:c.-21+35G>A ENSP00000496401.1:n.-21+35G>A
ENST00000646965.1:c.-47+1457G>A ENSP00000496456.1:n.-47+1457G>A
ENST00000382564.6:c.55+35G>A ENSP00000372005.2:n.55+35G>A
ENST00000469657.5:c.55+35G>A ENSP00000418058.1:n.55+35G>A
ENST00000472504.1:n.262G>A
ENST00000478723.5:n.194+35G>A
ENST00000479269.5:c.-21+35G>A ENSP00000419191.1:n.-21+35G>A
ENST00000482363.1:n.216+35G>A
ENST00000485675.1:n.129-47G>A
ENST00000486355.1:c.55+35G>A ENSP00000419991.1:n.55+35G>A
ENST00000491873.5:c.-20-47G>A ENSP00000420767.1:n.-20-47G>A
NM_001190233.1:c.-21+35G>A NP_001177162.1:n.-21+35G>A
NM_145261.3:c.55+35G>A NP_660304.1:n.55+35G>A
NR_033721.1:n.176-47G>A
NR_033722.1:n.227+35G>A
NR_033723.1:n.227+35G>A
NR_046073.1:n.175+1457G>A
NM_145261.4:c.55+35G>A MANE Select NP_660304.1:n.55+35G>A
NM_001190233.2:c.-21+35G>A NP_001177162.1:n.-21+35G>A
NR_033721.2:n.138-47G>A
NR_033722.2:n.189+35G>A