Canonical Allele Identifier: CA437196537

Gene: DNAJC19

Linked Data

• MyVariant Identifiers: chr3:g.180704742T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180986954T>A , CM000665.2:g.180986954T>A	GRCh38
NC_000003.11:g.180704742T>A , CM000665.1:g.180704742T>A	GRCh37
NC_000003.10:g.182187436T>A	NCBI36
NG_022933.1:g.7821A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.269A>T
ENST00000482363.2:n.1365A>T
ENST00000485675.2:n.1359A>T
ENST00000688055.1:c.198A>T	ENSP00000508688.1:p.Ile66=
ENST00000382564.8:c.198A>T MANE Select	ENSP00000372005.2:p.Ile66=
ENST00000643241.1:c.123A>T	ENSP00000496401.1:p.Ile41=
ENST00000646965.1:c.-46-958A>T	ENSP00000496456.1:n.-46-958A>T
ENST00000382564.6:c.198A>T	ENSP00000372005.2:p.Ile66=
ENST00000469657.5:c.130-958A>T	ENSP00000418058.1:n.130-958A>T
ENST00000478723.5:n.337A>T
ENST00000479269.5:c.123A>T	ENSP00000419191.1:p.Ile41=
ENST00000485675.1:n.1271A>T
ENST00000486355.1:c.154+44A>T	ENSP00000419991.1:n.154+44A>T
ENST00000491873.5:c.123A>T	ENSP00000420767.1:p.Ile41=
NM_001190233.1:c.123A>T	NP_001177162.1:p.Ile41=
NM_145261.3:c.198A>T	NP_660304.1:p.Ile66=
NR_033721.1:n.318A>T
NR_033722.1:n.302-958A>T
NR_033723.1:n.326+44A>T
NR_046073.1:n.176-958A>T
NM_145261.4:c.198A>T MANE Select	NP_660304.1:p.Ile66=
NM_001190233.2:c.123A>T	NP_001177162.1:p.Ile41=
NR_033721.2:n.280A>T
NR_033722.2:n.264-958A>T