Canonical Allele Identifier: CA89106300

Gene: DNAJC19

Linked Data

• dbSNP Id: rs774343049
• MyVariant Identifiers: chr3:g.180701875T>C (hg19) ; chr3:g.180984087T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180984087T>C , CM000665.2:g.180984087T>C	GRCh38
NC_000003.11:g.180701875T>C , CM000665.1:g.180701875T>C	GRCh37
NC_000003.10:g.182184569T>C	NCBI36
NG_022933.1:g.10688A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000482363.2:n.3017A>G
ENST00000688055.1:c.*1831A>G	ENSP00000508688.1:n.*1831A>G
ENST00000382564.8:c.*553A>G MANE Select	ENSP00000372005.2:n.*553A>G
ENST00000382564.6:c.*553A>G	ENSP00000372005.2:n.*553A>G
ENST00000469657.5:c.*680A>G	ENSP00000418058.1:n.*680A>G
NM_001190233.1:c.*553A>G	NP_001177162.1:n.*553A>G
NM_145261.3:c.*553A>G	NP_660304.1:n.*553A>G
NR_033721.1:n.1024A>G
NR_033722.1:n.996A>G
NR_033723.1:n.1021A>G
NR_046073.1:n.870A>G
NM_145261.4:c.*553A>G MANE Select	NP_660304.1:n.*553A>G
NM_001190233.2:c.*553A>G	NP_001177162.1:n.*553A>G
NR_033721.2:n.986A>G
NR_033722.2:n.958A>G