Canonical Allele Identifier: CA2668678444

Gene: DNAJC19

Linked Data

• gnomAD v4: 3-180986894-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180986894T>C , CM000665.2:g.180986894T>C	GRCh38
NC_000003.11:g.180704682T>C , CM000665.1:g.180704682T>C	GRCh37
NC_000003.10:g.182187376T>C	NCBI36
NG_022933.1:g.7881A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.280+49A>G
ENST00000482363.2:n.1425A>G
ENST00000485675.2:n.1419A>G
ENST00000688055.1:c.209+49A>G	ENSP00000508688.1:n.209+49A>G
ENST00000382564.8:c.209+49A>G MANE Select	ENSP00000372005.2:n.209+49A>G
ENST00000643241.1:c.129+54A>G	ENSP00000496401.1:n.129+54A>G
ENST00000646965.1:c.-46-898A>G	ENSP00000496456.1:n.-46-898A>G
ENST00000382564.6:c.209+49A>G	ENSP00000372005.2:n.209+49A>G
ENST00000469657.5:c.130-898A>G	ENSP00000418058.1:n.130-898A>G
ENST00000478723.5:n.348+49A>G
ENST00000479269.5:c.134+49A>G	ENSP00000419191.1:n.134+49A>G
ENST00000485675.1:n.1331A>G
ENST00000486355.1:c.154+104A>G	ENSP00000419991.1:n.154+104A>G
ENST00000491873.5:c.134+49A>G	ENSP00000420767.1:n.134+49A>G
NM_001190233.1:c.134+49A>G	NP_001177162.1:n.134+49A>G
NM_145261.3:c.209+49A>G	NP_660304.1:n.209+49A>G
NR_033721.1:n.329+49A>G
NR_033722.1:n.302-898A>G
NR_033723.1:n.326+104A>G
NR_046073.1:n.176-898A>G
NM_145261.4:c.209+49A>G MANE Select	NP_660304.1:n.209+49A>G
NM_001190233.2:c.134+49A>G	NP_001177162.1:n.134+49A>G
NR_033721.2:n.291+49A>G
NR_033722.2:n.264-898A>G