Canonical Allele Identifier: CA1424460279

Gene: DNAJC19

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180986909A= , CM000665.2:g.180986909A=	GRCh38
NC_000003.11:g.180704697A= , CM000665.1:g.180704697A=	GRCh37
NC_000003.10:g.182187391A=	NCBI36
NG_022933.1:g.7866T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.280+34T=
ENST00000482363.2:n.1410T=
ENST00000485675.2:n.1404T=
ENST00000688055.1:c.209+34T=	ENSP00000508688.1:n.209+34T=
ENST00000382564.8:c.209+34T= MANE Select	ENSP00000372005.2:n.209+34T=
ENST00000643241.1:c.129+39T=	ENSP00000496401.1:n.129+39T=
ENST00000646965.1:c.-46-913T=	ENSP00000496456.1:n.-46-913T=
ENST00000382564.6:c.209+34T=	ENSP00000372005.2:n.209+34T=
ENST00000469657.5:c.130-913T=	ENSP00000418058.1:n.130-913T=
ENST00000478723.5:n.348+34T=
ENST00000479269.5:c.134+34T=	ENSP00000419191.1:n.134+34T=
ENST00000485675.1:n.1316T=
ENST00000486355.1:c.154+89T=	ENSP00000419991.1:n.154+89T=
ENST00000491873.5:c.134+34T=	ENSP00000420767.1:n.134+34T=
NM_001190233.1:c.134+34T=	NP_001177162.1:n.134+34T=
NM_145261.3:c.209+34T=	NP_660304.1:n.209+34T=
NR_033721.1:n.329+34T=
NR_033722.1:n.302-913T=
NR_033723.1:n.326+89T=
NR_046073.1:n.176-913T=
NM_145261.4:c.209+34T= MANE Select	NP_660304.1:n.209+34T=
NM_001190233.2:c.134+34T=	NP_001177162.1:n.134+34T=
NR_033721.2:n.291+34T=
NR_033722.2:n.264-913T=