Canonical Allele Identifier: CA355472467

Gene: DNAJC19

Linked Data

• MyVariant Identifiers: chr3:g.180704764G>C (hg19) ; chr3:g.180986976G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180986976G>C , CM000665.2:g.180986976G>C	GRCh38
NC_000003.11:g.180704764G>C , CM000665.1:g.180704764G>C	GRCh37
NC_000003.10:g.182187458G>C	NCBI36
NG_022933.1:g.7799C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.247C>G
ENST00000482363.2:n.1343C>G
ENST00000485675.2:n.1337C>G
ENST00000688055.1:c.176C>G	ENSP00000508688.1:p.Thr59Arg
ENST00000382564.8:c.176C>G MANE Select	ENSP00000372005.2:p.Thr59Arg
ENST00000643241.1:c.101C>G	ENSP00000496401.1:p.Thr34Arg
ENST00000646965.1:c.-46-980C>G	ENSP00000496456.1:n.-46-980C>G
ENST00000382564.6:c.176C>G	ENSP00000372005.2:p.Thr59Arg
ENST00000469657.5:c.130-980C>G	ENSP00000418058.1:n.130-980C>G
ENST00000478723.5:n.315C>G
ENST00000479269.5:c.101C>G	ENSP00000419191.1:p.Thr34Arg
ENST00000485675.1:n.1249C>G
ENST00000486355.1:c.154+22C>G	ENSP00000419991.1:n.154+22C>G
ENST00000491873.5:c.101C>G	ENSP00000420767.1:p.Thr34Arg
NM_001190233.1:c.101C>G	NP_001177162.1:p.Thr34Arg
NM_145261.3:c.176C>G	NP_660304.1:p.Thr59Arg
NR_033721.1:n.296C>G
NR_033722.1:n.302-980C>G
NR_033723.1:n.326+22C>G
NR_046073.1:n.176-980C>G
NM_145261.4:c.176C>G MANE Select	NP_660304.1:p.Thr59Arg
NM_001190233.2:c.101C>G	NP_001177162.1:p.Thr34Arg
NR_033721.2:n.258C>G
NR_033722.2:n.264-980C>G