Canonical Allele Identifier: CA355472441

Gene: DNAJC19

Linked Data

• ClinVar Variation Id: 3084527
• ClinVar RCV Id: RCV004379407
• dbSNP Id: rs1435505055
• gnomAD v3: 3-180986964-G-A
• gnomAD v4: 3-180986964-G-A
• MyVariant Identifiers: chr3:g.180704752G>A (hg19) ; chr3:g.180986964G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180986964G>A , CM000665.2:g.180986964G>A	GRCh38
NC_000003.11:g.180704752G>A , CM000665.1:g.180704752G>A	GRCh37
NC_000003.10:g.182187446G>A	NCBI36
NG_022933.1:g.7811C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.259C>T
ENST00000482363.2:n.1355C>T
ENST00000485675.2:n.1349C>T
ENST00000688055.1:c.188C>T	ENSP00000508688.1:p.Ala63Val
ENST00000382564.8:c.188C>T MANE Select	ENSP00000372005.2:p.Ala63Val
ENST00000643241.1:c.113C>T	ENSP00000496401.1:p.Ala38Val
ENST00000646965.1:c.-46-968C>T	ENSP00000496456.1:n.-46-968C>T
ENST00000382564.6:c.188C>T	ENSP00000372005.2:p.Ala63Val
ENST00000469657.5:c.130-968C>T	ENSP00000418058.1:n.130-968C>T
ENST00000478723.5:n.327C>T
ENST00000479269.5:c.113C>T	ENSP00000419191.1:p.Ala38Val
ENST00000485675.1:n.1261C>T
ENST00000486355.1:c.154+34C>T	ENSP00000419991.1:n.154+34C>T
ENST00000491873.5:c.113C>T	ENSP00000420767.1:p.Ala38Val
NM_001190233.1:c.113C>T	NP_001177162.1:p.Ala38Val
NM_145261.3:c.188C>T	NP_660304.1:p.Ala63Val
NR_033721.1:n.308C>T
NR_033722.1:n.302-968C>T
NR_033723.1:n.326+34C>T
NR_046073.1:n.176-968C>T
NM_145261.4:c.188C>T MANE Select	NP_660304.1:p.Ala63Val
NM_001190233.2:c.113C>T	NP_001177162.1:p.Ala38Val
NR_033721.2:n.270C>T
NR_033722.2:n.264-968C>T