Canonical Allele Identifier: CA355472426

Gene: DNAJC19

Linked Data

• gnomAD v4: 3-180986956-T-C
• MyVariant Identifiers: chr3:g.180704744T>C (hg19) ; chr3:g.180986956T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180986956T>C , CM000665.2:g.180986956T>C	GRCh38
NC_000003.11:g.180704744T>C , CM000665.1:g.180704744T>C	GRCh37
NC_000003.10:g.182187438T>C	NCBI36
NG_022933.1:g.7819A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.267A>G
ENST00000482363.2:n.1363A>G
ENST00000485675.2:n.1357A>G
ENST00000688055.1:c.196A>G	ENSP00000508688.1:p.Ile66Val
ENST00000382564.8:c.196A>G MANE Select	ENSP00000372005.2:p.Ile66Val
ENST00000643241.1:c.121A>G	ENSP00000496401.1:p.Ile41Val
ENST00000646965.1:c.-46-960A>G	ENSP00000496456.1:n.-46-960A>G
ENST00000382564.6:c.196A>G	ENSP00000372005.2:p.Ile66Val
ENST00000469657.5:c.130-960A>G	ENSP00000418058.1:n.130-960A>G
ENST00000478723.5:n.335A>G
ENST00000479269.5:c.121A>G	ENSP00000419191.1:p.Ile41Val
ENST00000485675.1:n.1269A>G
ENST00000486355.1:c.154+42A>G	ENSP00000419991.1:n.154+42A>G
ENST00000491873.5:c.121A>G	ENSP00000420767.1:p.Ile41Val
NM_001190233.1:c.121A>G	NP_001177162.1:p.Ile41Val
NM_145261.3:c.196A>G	NP_660304.1:p.Ile66Val
NR_033721.1:n.316A>G
NR_033722.1:n.302-960A>G
NR_033723.1:n.326+42A>G
NR_046073.1:n.176-960A>G
NM_145261.4:c.196A>G MANE Select	NP_660304.1:p.Ile66Val
NM_001190233.2:c.121A>G	NP_001177162.1:p.Ile41Val
NR_033721.2:n.278A>G
NR_033722.2:n.264-960A>G