Canonical Allele Identifier: CA2717155

Gene: DNAJC19

Linked Data

• dbSNP Id: rs777376187
• ExAC: 3:180705925 A / G
• gnomAD v2: 3-180705925-A-G
• gnomAD v4: 3-180988137-A-G
• MyVariant Identifiers: chr3:g.180705925A>G (hg19) ; chr3:g.180988137A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180988137A>G , CM000665.2:g.180988137A>G	GRCh38
NC_000003.11:g.180705925A>G , CM000665.1:g.180705925A>G	GRCh37
NC_000003.10:g.182188619A>G	NCBI36
NG_022933.1:g.6638T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000478723.6:n.127-41T>C
ENST00000482363.2:n.223-41T>C
ENST00000485675.2:n.217-41T>C
ENST00000688055.1:c.56-41T>C	ENSP00000508688.1:n.56-41T>C
ENST00000382564.8:c.56-41T>C MANE Select	ENSP00000372005.2:n.56-41T>C
ENST00000643241.1:c.-20-41T>C	ENSP00000496401.1:n.-20-41T>C
ENST00000646965.1:c.-47+1463T>C	ENSP00000496456.1:n.-47+1463T>C
ENST00000382564.6:c.56-41T>C	ENSP00000372005.2:n.56-41T>C
ENST00000469657.5:c.56-41T>C	ENSP00000418058.1:n.56-41T>C
ENST00000472504.1:n.268T>C
ENST00000478723.5:n.195-41T>C
ENST00000479269.5:c.-20-41T>C	ENSP00000419191.1:n.-20-41T>C
ENST00000482363.1:n.217-41T>C
ENST00000485675.1:n.129-41T>C
ENST00000486355.1:c.56-41T>C	ENSP00000419991.1:n.56-41T>C
ENST00000491873.5:c.-20-41T>C	ENSP00000420767.1:n.-20-41T>C
NM_001190233.1:c.-20-41T>C	NP_001177162.1:n.-20-41T>C
NM_145261.3:c.56-41T>C	NP_660304.1:n.56-41T>C
NR_033721.1:n.176-41T>C
NR_033722.1:n.228-41T>C
NR_033723.1:n.228-41T>C
NR_046073.1:n.175+1463T>C
NM_145261.4:c.56-41T>C MANE Select	NP_660304.1:n.56-41T>C
NM_001190233.2:c.-20-41T>C	NP_001177162.1:n.-20-41T>C
NR_033721.2:n.138-41T>C
NR_033722.2:n.190-41T>C