Canonical Allele Identifier: CA1424460281

Gene: DNAJC19

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180986913A= , CM000665.2:g.180986913A=	GRCh38
NC_000003.11:g.180704701A= , CM000665.1:g.180704701A=	GRCh37
NC_000003.10:g.182187395A=	NCBI36
NG_022933.1:g.7862T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.280+30T=
ENST00000482363.2:n.1406T=
ENST00000485675.2:n.1400T=
ENST00000688055.1:c.209+30T=	ENSP00000508688.1:n.209+30T=
ENST00000382564.8:c.209+30T= MANE Select	ENSP00000372005.2:n.209+30T=
ENST00000643241.1:c.129+35T=	ENSP00000496401.1:n.129+35T=
ENST00000646965.1:c.-46-917T=	ENSP00000496456.1:n.-46-917T=
ENST00000382564.6:c.209+30T=	ENSP00000372005.2:n.209+30T=
ENST00000469657.5:c.130-917T=	ENSP00000418058.1:n.130-917T=
ENST00000478723.5:n.348+30T=
ENST00000479269.5:c.134+30T=	ENSP00000419191.1:n.134+30T=
ENST00000485675.1:n.1312T=
ENST00000486355.1:c.154+85T=	ENSP00000419991.1:n.154+85T=
ENST00000491873.5:c.134+30T=	ENSP00000420767.1:n.134+30T=
NM_001190233.1:c.134+30T=	NP_001177162.1:n.134+30T=
NM_145261.3:c.209+30T=	NP_660304.1:n.209+30T=
NR_033721.1:n.329+30T=
NR_033722.1:n.302-917T=
NR_033723.1:n.326+85T=
NR_046073.1:n.176-917T=
NM_145261.4:c.209+30T= MANE Select	NP_660304.1:n.209+30T=
NM_001190233.2:c.134+30T=	NP_001177162.1:n.134+30T=
NR_033721.2:n.291+30T=
NR_033722.2:n.264-917T=