Canonical Allele Identifier: CA355472515

Gene: DNAJC19

Linked Data

• gnomAD v4: 3-180986996-A-T
• MyVariant Identifiers: chr3:g.180704784A>T (hg19) ; chr3:g.180986996A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180986996A>T , CM000665.2:g.180986996A>T	GRCh38
NC_000003.11:g.180704784A>T , CM000665.1:g.180704784A>T	GRCh37
NC_000003.10:g.182187478A>T	NCBI36
NG_022933.1:g.7779T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.227T>A
ENST00000482363.2:n.1323T>A
ENST00000485675.2:n.1317T>A
ENST00000688055.1:c.156T>A	ENSP00000508688.1:p.Gly52=
ENST00000382564.8:c.156T>A MANE Select	ENSP00000372005.2:p.Gly52=
ENST00000643241.1:c.81T>A	ENSP00000496401.1:p.Gly27=
ENST00000646965.1:c.-46-1000T>A	ENSP00000496456.1:n.-46-1000T>A
ENST00000382564.6:c.156T>A	ENSP00000372005.2:p.Gly52=
ENST00000469657.5:c.130-1000T>A	ENSP00000418058.1:n.130-1000T>A
ENST00000478723.5:n.295T>A
ENST00000479269.5:c.81T>A	ENSP00000419191.1:p.Gly27=
ENST00000485675.1:n.1229T>A
ENST00000486355.1:c.154+2T>A	ENSP00000419991.1:n.154+2T>A
ENST00000491873.5:c.81T>A	ENSP00000420767.1:p.Gly27=
NM_001190233.1:c.81T>A	NP_001177162.1:p.Gly27=
NM_145261.3:c.156T>A	NP_660304.1:p.Gly52=
NR_033721.1:n.276T>A
NR_033722.1:n.302-1000T>A
NR_033723.1:n.326+2T>A
NR_046073.1:n.176-1000T>A
NM_145261.4:c.156T>A MANE Select	NP_660304.1:p.Gly52=
NM_001190233.2:c.81T>A	NP_001177162.1:p.Gly27=
NR_033721.2:n.238T>A
NR_033722.2:n.264-1000T>A