Canonical Allele Identifier: CA1057000660

Gene: DNAJC19

Linked Data

• dbSNP Id: rs1714761204
• gnomAD v3: 3-180984052-T-C
• gnomAD v4: 3-180984052-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180984052T>C , CM000665.2:g.180984052T>C	GRCh38
NC_000003.11:g.180701840T>C , CM000665.1:g.180701840T>C	GRCh37
NC_000003.10:g.182184534T>C	NCBI36
NG_022933.1:g.10723A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482363.2:n.3052A>G
ENST00000688055.1:c.*1866A>G	ENSP00000508688.1:n.*1866A>G
ENST00000382564.8:c.*588A>G MANE Select	ENSP00000372005.2:n.*588A>G
ENST00000382564.6:c.*588A>G	ENSP00000372005.2:n.*588A>G
ENST00000469657.5:c.*715A>G	ENSP00000418058.1:n.*715A>G
NM_001190233.1:c.*588A>G	NP_001177162.1:n.*588A>G
NM_145261.3:c.*588A>G	NP_660304.1:n.*588A>G
NR_033721.1:n.1059A>G
NR_033722.1:n.1031A>G
NR_033723.1:n.1056A>G
NR_046073.1:n.905A>G
NM_145261.4:c.*588A>G MANE Select	NP_660304.1:n.*588A>G
NM_001190233.2:c.*588A>G	NP_001177162.1:n.*588A>G
NR_033721.2:n.1021A>G
NR_033722.2:n.993A>G