Canonical Allele Identifier: CA355472399

Gene: DNAJC19

Linked Data

• MyVariant Identifiers: chr3:g.180704731C>A (hg19) ; chr3:g.180986943C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180986943C>A , CM000665.2:g.180986943C>A	GRCh38
NC_000003.11:g.180704731C>A , CM000665.1:g.180704731C>A	GRCh37
NC_000003.10:g.182187425C>A	NCBI36
NG_022933.1:g.7832G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.280G>T
ENST00000482363.2:n.1376G>T
ENST00000485675.2:n.1370G>T
ENST00000688055.1:c.209G>T	ENSP00000508688.1:p.Ser70Ile
ENST00000382564.8:c.209G>T MANE Select	ENSP00000372005.2:p.Ser70Ile
ENST00000643241.1:c.129+5G>T	ENSP00000496401.1:n.129+5G>T
ENST00000646965.1:c.-46-947G>T	ENSP00000496456.1:n.-46-947G>T
ENST00000382564.6:c.209G>T	ENSP00000372005.2:p.Ser70Ile
ENST00000469657.5:c.130-947G>T	ENSP00000418058.1:n.130-947G>T
ENST00000478723.5:n.348G>T
ENST00000479269.5:c.134G>T	ENSP00000419191.1:p.Ser45Ile
ENST00000485675.1:n.1282G>T
ENST00000486355.1:c.154+55G>T	ENSP00000419991.1:n.154+55G>T
ENST00000491873.5:c.134G>T	ENSP00000420767.1:p.Ser45Ile
NM_001190233.1:c.134G>T	NP_001177162.1:p.Ser45Ile
NM_145261.3:c.209G>T	NP_660304.1:p.Ser70Ile
NR_033721.1:n.329G>T
NR_033722.1:n.302-947G>T
NR_033723.1:n.326+55G>T
NR_046073.1:n.176-947G>T
NM_145261.4:c.209G>T MANE Select	NP_660304.1:p.Ser70Ile
NM_001190233.2:c.134G>T	NP_001177162.1:p.Ser45Ile
NR_033721.2:n.291G>T
NR_033722.2:n.264-947G>T