Canonical Allele Identifier: CA1424458962

Gene: DNAJC19

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180984070_180984073delinsTAAA , CM000665.2:g.180984070_180984073delinsTAAA	GRCh38
NC_000003.11:g.180701858_180701861delinsTAAA , CM000665.1:g.180701858_180701861delinsTAAA	GRCh37
NC_000003.10:g.182184552_182184555delinsTAAA	NCBI36
NG_022933.1:g.10702_10705delinsTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482363.2:n.3031_3034delinsTTTA
ENST00000688055.1:c.*1845_*1848delinsTTTA	ENSP00000508688.1:n.*1845_*1848delinsTTTA
ENST00000382564.8:c.*567_*570delinsTTTA MANE Select	ENSP00000372005.2:n.*567_*570delinsTTTA
ENST00000382564.6:c.*567_*570delinsTTTA	ENSP00000372005.2:n.*567_*570delinsTTTA
ENST00000469657.5:c.*694_*697delinsTTTA	ENSP00000418058.1:n.*694_*697delinsTTTA
NM_001190233.1:c.*567_*570delinsTTTA	NP_001177162.1:n.*567_*570delinsTTTA
NM_145261.3:c.*567_*570delinsTTTA	NP_660304.1:n.*567_*570delinsTTTA
NR_033721.1:n.1038_1041delinsTTTA
NR_033722.1:n.1010_1013delinsTTTA
NR_033723.1:n.1035_1038delinsTTTA
NR_046073.1:n.884_887delinsTTTA
NM_145261.4:c.*567_*570delinsTTTA MANE Select	NP_660304.1:n.*567_*570delinsTTTA
NM_001190233.2:c.*567_*570delinsTTTA	NP_001177162.1:n.*567_*570delinsTTTA
NR_033721.2:n.1000_1003delinsTTTA
NR_033722.2:n.972_975delinsTTTA