Canonical Allele Identifier: CA1424460329

Gene: DNAJC19

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180987025G= , CM000665.2:g.180987025G=	GRCh38
NC_000003.11:g.180704813G= , CM000665.1:g.180704813G=	GRCh37
NC_000003.10:g.182187507G=	NCBI36
NG_022933.1:g.7750C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.201-3C=
ENST00000482363.2:n.1294C=
ENST00000485675.2:n.1288C=
ENST00000688055.1:c.130-3C=	ENSP00000508688.1:n.130-3C=
ENST00000382564.8:c.130-3C= MANE Select	ENSP00000372005.2:n.130-3C=
ENST00000643241.1:c.55-3C=	ENSP00000496401.1:n.55-3C=
ENST00000646965.1:c.-46-1029C=	ENSP00000496456.1:n.-46-1029C=
ENST00000382564.6:c.130-3C=	ENSP00000372005.2:n.130-3C=
ENST00000469657.5:c.129+998C=	ENSP00000418058.1:n.129+998C=
ENST00000478723.5:n.269-3C=
ENST00000479269.5:c.55-3C=	ENSP00000419191.1:n.55-3C=
ENST00000485675.1:n.1200C=
ENST00000486355.1:c.130-3C=	ENSP00000419991.1:n.130-3C=
ENST00000491873.5:c.55-3C=	ENSP00000420767.1:n.55-3C=
NM_001190233.1:c.55-3C=	NP_001177162.1:n.55-3C=
NM_145261.3:c.130-3C=	NP_660304.1:n.130-3C=
NR_033721.1:n.250-3C=
NR_033722.1:n.301+998C=
NR_033723.1:n.302-3C=
NR_046073.1:n.176-1029C=
NM_145261.4:c.130-3C= MANE Select	NP_660304.1:n.130-3C=
NM_001190233.2:c.55-3C=	NP_001177162.1:n.55-3C=
NR_033721.2:n.212-3C=
NR_033722.2:n.263+998C=