Canonical Allele Identifier: CA437196561

Gene: DNAJC19

Linked Data

• MyVariant Identifiers: chr3:g.180704748T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180986960T>G , CM000665.2:g.180986960T>G	GRCh38
NC_000003.11:g.180704748T>G , CM000665.1:g.180704748T>G	GRCh37
NC_000003.10:g.182187442T>G	NCBI36
NG_022933.1:g.7815A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.263A>C
ENST00000482363.2:n.1359A>C
ENST00000485675.2:n.1353A>C
ENST00000688055.1:c.192A>C	ENSP00000508688.1:p.Ala64=
ENST00000382564.8:c.192A>C MANE Select	ENSP00000372005.2:p.Ala64=
ENST00000643241.1:c.117A>C	ENSP00000496401.1:p.Ala39=
ENST00000646965.1:c.-46-964A>C	ENSP00000496456.1:n.-46-964A>C
ENST00000382564.6:c.192A>C	ENSP00000372005.2:p.Ala64=
ENST00000469657.5:c.130-964A>C	ENSP00000418058.1:n.130-964A>C
ENST00000478723.5:n.331A>C
ENST00000479269.5:c.117A>C	ENSP00000419191.1:p.Ala39=
ENST00000485675.1:n.1265A>C
ENST00000486355.1:c.154+38A>C	ENSP00000419991.1:n.154+38A>C
ENST00000491873.5:c.117A>C	ENSP00000420767.1:p.Ala39=
NM_001190233.1:c.117A>C	NP_001177162.1:p.Ala39=
NM_145261.3:c.192A>C	NP_660304.1:p.Ala64=
NR_033721.1:n.312A>C
NR_033722.1:n.302-964A>C
NR_033723.1:n.326+38A>C
NR_046073.1:n.176-964A>C
NM_145261.4:c.192A>C MANE Select	NP_660304.1:p.Ala64=
NM_001190233.2:c.117A>C	NP_001177162.1:p.Ala39=
NR_033721.2:n.274A>C
NR_033722.2:n.264-964A>C