Canonical Allele Identifier: CA1424460283

Gene: DNAJC19

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180986920A= , CM000665.2:g.180986920A=	GRCh38
NC_000003.11:g.180704708A= , CM000665.1:g.180704708A=	GRCh37
NC_000003.10:g.182187402A=	NCBI36
NG_022933.1:g.7855T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.280+23T=
ENST00000482363.2:n.1399T=
ENST00000485675.2:n.1393T=
ENST00000688055.1:c.209+23T=	ENSP00000508688.1:n.209+23T=
ENST00000382564.8:c.209+23T= MANE Select	ENSP00000372005.2:n.209+23T=
ENST00000643241.1:c.129+28T=	ENSP00000496401.1:n.129+28T=
ENST00000646965.1:c.-46-924T=	ENSP00000496456.1:n.-46-924T=
ENST00000382564.6:c.209+23T=	ENSP00000372005.2:n.209+23T=
ENST00000469657.5:c.130-924T=	ENSP00000418058.1:n.130-924T=
ENST00000478723.5:n.348+23T=
ENST00000479269.5:c.134+23T=	ENSP00000419191.1:n.134+23T=
ENST00000485675.1:n.1305T=
ENST00000486355.1:c.154+78T=	ENSP00000419991.1:n.154+78T=
ENST00000491873.5:c.134+23T=	ENSP00000420767.1:n.134+23T=
NM_001190233.1:c.134+23T=	NP_001177162.1:n.134+23T=
NM_145261.3:c.209+23T=	NP_660304.1:n.209+23T=
NR_033721.1:n.329+23T=
NR_033722.1:n.302-924T=
NR_033723.1:n.326+78T=
NR_046073.1:n.176-924T=
NM_145261.4:c.209+23T= MANE Select	NP_660304.1:n.209+23T=
NM_001190233.2:c.134+23T=	NP_001177162.1:n.134+23T=
NR_033721.2:n.291+23T=
NR_033722.2:n.264-924T=