Canonical Allele Identifier: CA1424460795

Gene: DNAJC19

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180988137A= , CM000665.2:g.180988137A=	GRCh38
NC_000003.11:g.180705925A= , CM000665.1:g.180705925A=	GRCh37
NC_000003.10:g.182188619A=	NCBI36
NG_022933.1:g.6638T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.127-41T=
ENST00000482363.2:n.223-41T=
ENST00000485675.2:n.217-41T=
ENST00000688055.1:c.56-41T=	ENSP00000508688.1:n.56-41T=
ENST00000382564.8:c.56-41T= MANE Select	ENSP00000372005.2:n.56-41T=
ENST00000643241.1:c.-20-41T=	ENSP00000496401.1:n.-20-41T=
ENST00000646965.1:c.-47+1463T=	ENSP00000496456.1:n.-47+1463T=
ENST00000382564.6:c.56-41T=	ENSP00000372005.2:n.56-41T=
ENST00000469657.5:c.56-41T=	ENSP00000418058.1:n.56-41T=
ENST00000472504.1:n.268T=
ENST00000478723.5:n.195-41T=
ENST00000479269.5:c.-20-41T=	ENSP00000419191.1:n.-20-41T=
ENST00000482363.1:n.217-41T=
ENST00000485675.1:n.129-41T=
ENST00000486355.1:c.56-41T=	ENSP00000419991.1:n.56-41T=
ENST00000491873.5:c.-20-41T=	ENSP00000420767.1:n.-20-41T=
NM_001190233.1:c.-20-41T=	NP_001177162.1:n.-20-41T=
NM_145261.3:c.56-41T=	NP_660304.1:n.56-41T=
NR_033721.1:n.176-41T=
NR_033722.1:n.228-41T=
NR_033723.1:n.228-41T=
NR_046073.1:n.175+1463T=
NM_145261.4:c.56-41T= MANE Select	NP_660304.1:n.56-41T=
NM_001190233.2:c.-20-41T=	NP_001177162.1:n.-20-41T=
NR_033721.2:n.138-41T=
NR_033722.2:n.190-41T=