Canonical Allele Identifier: CA1424460839
Gene: DNAJC19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180988250A= , CM000665.2:g.180988250A= GRCh38
NC_000003.11:g.180706038A= , CM000665.1:g.180706038A= GRCh37
NC_000003.10:g.182188732A= NCBI36
NG_022933.1:g.6525T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000478723.6:n.75-21T=
ENST00000482363.2:n.171-21T=
ENST00000485675.2:n.165-21T=
ENST00000688055.1:c.4-21T= ENSP00000508688.1:n.4-21T=
ENST00000382564.8:c.4-21T= MANE Select ENSP00000372005.2:n.4-21T=
ENST00000643241.1:c.-72-21T= ENSP00000496401.1:n.-72-21T=
ENST00000646965.1:c.-47+1350T= ENSP00000496456.1:n.-47+1350T=
ENST00000382564.6:c.4-21T= ENSP00000372005.2:n.4-21T=
ENST00000469657.5:c.4-21T= ENSP00000418058.1:n.4-21T=
ENST00000472504.1:n.176-21T=
ENST00000478723.5:n.143-21T=
ENST00000479269.5:c.-72-21T= ENSP00000419191.1:n.-72-21T=
ENST00000482363.1:n.165-21T=
ENST00000485675.1:n.129-154T=
ENST00000486355.1:c.4-21T= ENSP00000419991.1:n.4-21T=
ENST00000491873.5:c.-20-154T= ENSP00000420767.1:n.-20-154T=
NM_001190233.1:c.-72-21T= NP_001177162.1:n.-72-21T=
NM_145261.3:c.4-21T= NP_660304.1:n.4-21T=
NR_033721.1:n.176-154T=
NR_033722.1:n.176-21T=
NR_033723.1:n.176-21T=
NR_046073.1:n.175+1350T=
NM_145261.4:c.4-21T= MANE Select NP_660304.1:n.4-21T=
NM_001190233.2:c.-72-21T= NP_001177162.1:n.-72-21T=
NR_033721.2:n.138-154T=
NR_033722.2:n.138-21T=