Canonical Allele Identifier: CA2717154

Gene: DNAJC19

Linked Data

• dbSNP Id: rs769449262
• ExAC: 3:180705922 C / T
• gnomAD v2: 3-180705922-C-T
• gnomAD v4: 3-180988134-C-T
• MyVariant Identifiers: chr3:g.180705922C>T (hg19) ; chr3:g.180988134C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180988134C>T , CM000665.2:g.180988134C>T	GRCh38
NC_000003.11:g.180705922C>T , CM000665.1:g.180705922C>T	GRCh37
NC_000003.10:g.182188616C>T	NCBI36
NG_022933.1:g.6641G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000478723.6:n.127-38G>A
ENST00000482363.2:n.223-38G>A
ENST00000485675.2:n.217-38G>A
ENST00000688055.1:c.56-38G>A	ENSP00000508688.1:n.56-38G>A
ENST00000382564.8:c.56-38G>A MANE Select	ENSP00000372005.2:n.56-38G>A
ENST00000643241.1:c.-20-38G>A	ENSP00000496401.1:n.-20-38G>A
ENST00000646965.1:c.-47+1466G>A	ENSP00000496456.1:n.-47+1466G>A
ENST00000382564.6:c.56-38G>A	ENSP00000372005.2:n.56-38G>A
ENST00000469657.5:c.56-38G>A	ENSP00000418058.1:n.56-38G>A
ENST00000472504.1:n.271G>A
ENST00000478723.5:n.195-38G>A
ENST00000479269.5:c.-20-38G>A	ENSP00000419191.1:n.-20-38G>A
ENST00000482363.1:n.217-38G>A
ENST00000485675.1:n.129-38G>A
ENST00000486355.1:c.56-38G>A	ENSP00000419991.1:n.56-38G>A
ENST00000491873.5:c.-20-38G>A	ENSP00000420767.1:n.-20-38G>A
NM_001190233.1:c.-20-38G>A	NP_001177162.1:n.-20-38G>A
NM_145261.3:c.56-38G>A	NP_660304.1:n.56-38G>A
NR_033721.1:n.176-38G>A
NR_033722.1:n.228-38G>A
NR_033723.1:n.228-38G>A
NR_046073.1:n.175+1466G>A
NM_145261.4:c.56-38G>A MANE Select	NP_660304.1:n.56-38G>A
NM_001190233.2:c.-20-38G>A	NP_001177162.1:n.-20-38G>A
NR_033721.2:n.138-38G>A
NR_033722.2:n.190-38G>A