Canonical Allele Identifier: CA1424460836
Gene: DNAJC19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180988242A= , CM000665.2:g.180988242A= GRCh38
NC_000003.11:g.180706030A= , CM000665.1:g.180706030A= GRCh37
NC_000003.10:g.182188724A= NCBI36
NG_022933.1:g.6533T=

Transcript Alleles

HGVS Amino-acid change
ENST00000478723.6:n.75-13T=
ENST00000482363.2:n.171-13T=
ENST00000485675.2:n.165-13T=
ENST00000688055.1:c.4-13T= ENSP00000508688.1:n.4-13T=
ENST00000382564.8:c.4-13T= MANE Select ENSP00000372005.2:n.4-13T=
ENST00000643241.1:c.-72-13T= ENSP00000496401.1:n.-72-13T=
ENST00000646965.1:c.-47+1358T= ENSP00000496456.1:n.-47+1358T=
ENST00000382564.6:c.4-13T= ENSP00000372005.2:n.4-13T=
ENST00000469657.5:c.4-13T= ENSP00000418058.1:n.4-13T=
ENST00000472504.1:n.176-13T=
ENST00000478723.5:n.143-13T=
ENST00000479269.5:c.-72-13T= ENSP00000419191.1:n.-72-13T=
ENST00000482363.1:n.165-13T=
ENST00000485675.1:n.129-146T=
ENST00000486355.1:c.4-13T= ENSP00000419991.1:n.4-13T=
ENST00000491873.5:c.-20-146T= ENSP00000420767.1:n.-20-146T=
NM_001190233.1:c.-72-13T= NP_001177162.1:n.-72-13T=
NM_145261.3:c.4-13T= NP_660304.1:n.4-13T=
NR_033721.1:n.176-146T=
NR_033722.1:n.176-13T=
NR_033723.1:n.176-13T=
NR_046073.1:n.175+1358T=
NM_145261.4:c.4-13T= MANE Select NP_660304.1:n.4-13T=
NM_001190233.2:c.-72-13T= NP_001177162.1:n.-72-13T=
NR_033721.2:n.138-146T=
NR_033722.2:n.138-13T=