Canonical Allele Identifier: CA437196582

Gene: DNAJC19

Linked Data

• MyVariant Identifiers: chr3:g.180704757C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180986969C>A , CM000665.2:g.180986969C>A	GRCh38
NC_000003.11:g.180704757C>A , CM000665.1:g.180704757C>A	GRCh37
NC_000003.10:g.182187451C>A	NCBI36
NG_022933.1:g.7806G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.254G>T
ENST00000482363.2:n.1350G>T
ENST00000485675.2:n.1344G>T
ENST00000688055.1:c.183G>T	ENSP00000508688.1:p.Arg61=
ENST00000382564.8:c.183G>T MANE Select	ENSP00000372005.2:p.Arg61=
ENST00000643241.1:c.108G>T	ENSP00000496401.1:p.Arg36=
ENST00000646965.1:c.-46-973G>T	ENSP00000496456.1:n.-46-973G>T
ENST00000382564.6:c.183G>T	ENSP00000372005.2:p.Arg61=
ENST00000469657.5:c.130-973G>T	ENSP00000418058.1:n.130-973G>T
ENST00000478723.5:n.322G>T
ENST00000479269.5:c.108G>T	ENSP00000419191.1:p.Arg36=
ENST00000485675.1:n.1256G>T
ENST00000486355.1:c.154+29G>T	ENSP00000419991.1:n.154+29G>T
ENST00000491873.5:c.108G>T	ENSP00000420767.1:p.Arg36=
NM_001190233.1:c.108G>T	NP_001177162.1:p.Arg36=
NM_145261.3:c.183G>T	NP_660304.1:p.Arg61=
NR_033721.1:n.303G>T
NR_033722.1:n.302-973G>T
NR_033723.1:n.326+29G>T
NR_046073.1:n.176-973G>T
NM_145261.4:c.183G>T MANE Select	NP_660304.1:p.Arg61=
NM_001190233.2:c.108G>T	NP_001177162.1:p.Arg36=
NR_033721.2:n.265G>T
NR_033722.2:n.264-973G>T