Canonical Allele Identifier: CA1424460800
Gene: DNAJC19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180988148T= , CM000665.2:g.180988148T= GRCh38
NC_000003.11:g.180705936T= , CM000665.1:g.180705936T= GRCh37
NC_000003.10:g.182188630T= NCBI36
NG_022933.1:g.6627A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000478723.6:n.126+30A=
ENST00000482363.2:n.222+30A=
ENST00000485675.2:n.216+30A=
ENST00000688055.1:c.55+30A= ENSP00000508688.1:n.55+30A=
ENST00000382564.8:c.55+30A= MANE Select ENSP00000372005.2:n.55+30A=
ENST00000643241.1:c.-21+30A= ENSP00000496401.1:n.-21+30A=
ENST00000646965.1:c.-47+1452A= ENSP00000496456.1:n.-47+1452A=
ENST00000382564.6:c.55+30A= ENSP00000372005.2:n.55+30A=
ENST00000469657.5:c.55+30A= ENSP00000418058.1:n.55+30A=
ENST00000472504.1:n.257A=
ENST00000478723.5:n.194+30A=
ENST00000479269.5:c.-21+30A= ENSP00000419191.1:n.-21+30A=
ENST00000482363.1:n.216+30A=
ENST00000485675.1:n.129-52A=
ENST00000486355.1:c.55+30A= ENSP00000419991.1:n.55+30A=
ENST00000491873.5:c.-20-52A= ENSP00000420767.1:n.-20-52A=
NM_001190233.1:c.-21+30A= NP_001177162.1:n.-21+30A=
NM_145261.3:c.55+30A= NP_660304.1:n.55+30A=
NR_033721.1:n.176-52A=
NR_033722.1:n.227+30A=
NR_033723.1:n.227+30A=
NR_046073.1:n.175+1452A=
NM_145261.4:c.55+30A= MANE Select NP_660304.1:n.55+30A=
NM_001190233.2:c.-21+30A= NP_001177162.1:n.-21+30A=
NR_033721.2:n.138-52A=
NR_033722.2:n.189+30A=