Canonical Allele Identifier: CA325277

Gene: DNAJC19

Linked Data

• ClinVar Variation Id: 214299
• ClinVar RCV Id: RCV000200698 ; RCV001393978 ; RCV002515392
• dbSNP Id: rs376891597
• ExAC: 3:180704758 C / T
• gnomAD v2: 3-180704758-C-T
• gnomAD v3: 3-180986970-C-T
• gnomAD v4: 3-180986970-C-T
• MyVariant Identifiers: chr3:g.180704758C>T (hg19) ; chr3:g.180986970C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180986970C>T , CM000665.2:g.180986970C>T	GRCh38
NC_000003.11:g.180704758C>T , CM000665.1:g.180704758C>T	GRCh37
NC_000003.10:g.182187452C>T	NCBI36
NG_022933.1:g.7805G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.253G>A
ENST00000482363.2:n.1349G>A
ENST00000485675.2:n.1343G>A
ENST00000688055.1:c.182G>A	ENSP00000508688.1:p.Arg61Gln
ENST00000382564.8:c.182G>A MANE Select	ENSP00000372005.2:p.Arg61Gln
ENST00000643241.1:c.107G>A	ENSP00000496401.1:p.Arg36Gln
ENST00000646965.1:c.-46-974G>A	ENSP00000496456.1:n.-46-974G>A
ENST00000382564.6:c.182G>A	ENSP00000372005.2:p.Arg61Gln
ENST00000469657.5:c.130-974G>A	ENSP00000418058.1:n.130-974G>A
ENST00000478723.5:n.321G>A
ENST00000479269.5:c.107G>A	ENSP00000419191.1:p.Arg36Gln
ENST00000485675.1:n.1255G>A
ENST00000486355.1:c.154+28G>A	ENSP00000419991.1:n.154+28G>A
ENST00000491873.5:c.107G>A	ENSP00000420767.1:p.Arg36Gln
NM_001190233.1:c.107G>A	NP_001177162.1:p.Arg36Gln
NM_145261.3:c.182G>A	NP_660304.1:p.Arg61Gln
NR_033721.1:n.302G>A
NR_033722.1:n.302-974G>A
NR_033723.1:n.326+28G>A
NR_046073.1:n.176-974G>A
NM_145261.4:c.182G>A MANE Select	NP_660304.1:p.Arg61Gln
NM_001190233.2:c.107G>A	NP_001177162.1:p.Arg36Gln
NR_033721.2:n.264G>A
NR_033722.2:n.264-974G>A