Canonical Allele Identifier: CA1057001818

Gene: DNAJC19

Linked Data

• dbSNP Id: rs1714940857
• gnomAD v3: 3-180986935-TA-T
• gnomAD v4: 3-180986935-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180986936del , CM000665.2:g.180986936del	GRCh38
NC_000003.11:g.180704724del , CM000665.1:g.180704724del	GRCh37
NC_000003.10:g.182187418del	NCBI36
NG_022933.1:g.7839del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.280+7del
ENST00000482363.2:n.1383del
ENST00000485675.2:n.1377del
ENST00000688055.1:c.209+7del	ENSP00000508688.1:n.209+7del
ENST00000382564.8:c.209+7del MANE Select	ENSP00000372005.2:n.209+7del
ENST00000643241.1:c.129+12del	ENSP00000496401.1:n.129+12del
ENST00000646965.1:c.-46-940del	ENSP00000496456.1:n.-46-940del
ENST00000382564.6:c.209+7del	ENSP00000372005.2:n.209+7del
ENST00000469657.5:c.130-940del	ENSP00000418058.1:n.130-940del
ENST00000478723.5:n.348+7del
ENST00000479269.5:c.134+7del	ENSP00000419191.1:n.134+7del
ENST00000485675.1:n.1289del
ENST00000486355.1:c.154+62del	ENSP00000419991.1:n.154+62del
ENST00000491873.5:c.134+7del	ENSP00000420767.1:n.134+7del
NM_001190233.1:c.134+7del	NP_001177162.1:n.134+7del
NM_145261.3:c.209+7del	NP_660304.1:n.209+7del
NR_033721.1:n.329+7del
NR_033722.1:n.302-940del
NR_033723.1:n.326+62del
NR_046073.1:n.176-940del
NM_145261.4:c.209+7del MANE Select	NP_660304.1:n.209+7del
NM_001190233.2:c.134+7del	NP_001177162.1:n.134+7del
NR_033721.2:n.291+7del
NR_033722.2:n.264-940del