Canonical Allele Identifier: CA355472502

Gene: DNAJC19

Linked Data

• MyVariant Identifiers: chr3:g.180704778A>T (hg19) ; chr3:g.180986990A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180986990A>T , CM000665.2:g.180986990A>T	GRCh38
NC_000003.11:g.180704778A>T , CM000665.1:g.180704778A>T	GRCh37
NC_000003.10:g.182187472A>T	NCBI36
NG_022933.1:g.7785T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.233T>A
ENST00000482363.2:n.1329T>A
ENST00000485675.2:n.1323T>A
ENST00000688055.1:c.162T>A	ENSP00000508688.1:p.Phe54Leu
ENST00000382564.8:c.162T>A MANE Select	ENSP00000372005.2:p.Phe54Leu
ENST00000643241.1:c.87T>A	ENSP00000496401.1:p.Phe29Leu
ENST00000646965.1:c.-46-994T>A	ENSP00000496456.1:n.-46-994T>A
ENST00000382564.6:c.162T>A	ENSP00000372005.2:p.Phe54Leu
ENST00000469657.5:c.130-994T>A	ENSP00000418058.1:n.130-994T>A
ENST00000478723.5:n.301T>A
ENST00000479269.5:c.87T>A	ENSP00000419191.1:p.Phe29Leu
ENST00000485675.1:n.1235T>A
ENST00000486355.1:c.154+8T>A	ENSP00000419991.1:n.154+8T>A
ENST00000491873.5:c.87T>A	ENSP00000420767.1:p.Phe29Leu
NM_001190233.1:c.87T>A	NP_001177162.1:p.Phe29Leu
NM_145261.3:c.162T>A	NP_660304.1:p.Phe54Leu
NR_033721.1:n.282T>A
NR_033722.1:n.302-994T>A
NR_033723.1:n.326+8T>A
NR_046073.1:n.176-994T>A
NM_145261.4:c.162T>A MANE Select	NP_660304.1:p.Phe54Leu
NM_001190233.2:c.87T>A	NP_001177162.1:p.Phe29Leu
NR_033721.2:n.244T>A
NR_033722.2:n.264-994T>A