Canonical Allele Identifier: CA2668679446

Gene: DNAJC19

Linked Data

• gnomAD v4: 3-180988158-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180988162del , CM000665.2:g.180988162del	GRCh38
NC_000003.11:g.180705950del , CM000665.1:g.180705950del	GRCh37
NC_000003.10:g.182188644del	NCBI36
NG_022933.1:g.6616del

Transcript Alleles

HGVS	Amino-acid change
ENST00000478723.6:n.126+19del
ENST00000482363.2:n.222+19del
ENST00000485675.2:n.216+19del
ENST00000688055.1:c.55+19del	ENSP00000508688.1:n.55+19del
ENST00000382564.8:c.55+19del MANE Select	ENSP00000372005.2:n.55+19del
ENST00000643241.1:c.-21+19del	ENSP00000496401.1:n.-21+19del
ENST00000646965.1:c.-47+1441del	ENSP00000496456.1:n.-47+1441del
ENST00000382564.6:c.55+19del	ENSP00000372005.2:n.55+19del
ENST00000469657.5:c.55+19del	ENSP00000418058.1:n.55+19del
ENST00000472504.1:n.246del
ENST00000478723.5:n.194+19del
ENST00000479269.5:c.-21+19del	ENSP00000419191.1:n.-21+19del
ENST00000482363.1:n.216+19del
ENST00000485675.1:n.129-63del
ENST00000486355.1:c.55+19del	ENSP00000419991.1:n.55+19del
ENST00000491873.5:c.-20-63del	ENSP00000420767.1:n.-20-63del
NM_001190233.1:c.-21+19del	NP_001177162.1:n.-21+19del
NM_145261.3:c.55+19del	NP_660304.1:n.55+19del
NR_033721.1:n.176-63del
NR_033722.1:n.227+19del
NR_033723.1:n.227+19del
NR_046073.1:n.175+1441del
NM_145261.4:c.55+19del MANE Select	NP_660304.1:n.55+19del
NM_001190233.2:c.-21+19del	NP_001177162.1:n.-21+19del
NR_033721.2:n.138-63del
NR_033722.2:n.189+19del