Canonical Allele Identifier: CA548508107

Gene: DNAJC19

Linked Data

• dbSNP Id: rs1210577749
• gnomAD v2: 3-180701874-G-A
• gnomAD v3: 3-180984086-G-A
• gnomAD v4: 3-180984086-G-A
• MyVariant Identifiers: chr3:g.180701874G>A (hg19) ; chr3:g.180984086G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180984086G>A , CM000665.2:g.180984086G>A	GRCh38
NC_000003.11:g.180701874G>A , CM000665.1:g.180701874G>A	GRCh37
NC_000003.10:g.182184568G>A	NCBI36
NG_022933.1:g.10689C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482363.2:n.3018C>T
ENST00000688055.1:c.*1832C>T	ENSP00000508688.1:n.*1832C>T
ENST00000382564.8:c.*554C>T MANE Select	ENSP00000372005.2:n.*554C>T
ENST00000382564.6:c.*554C>T	ENSP00000372005.2:n.*554C>T
ENST00000469657.5:c.*681C>T	ENSP00000418058.1:n.*681C>T
NM_001190233.1:c.*554C>T	NP_001177162.1:n.*554C>T
NM_145261.3:c.*554C>T	NP_660304.1:n.*554C>T
NR_033721.1:n.1025C>T
NR_033722.1:n.997C>T
NR_033723.1:n.1022C>T
NR_046073.1:n.871C>T
NM_145261.4:c.*554C>T MANE Select	NP_660304.1:n.*554C>T
NM_001190233.2:c.*554C>T	NP_001177162.1:n.*554C>T
NR_033721.2:n.987C>T
NR_033722.2:n.959C>T