Canonical Allele Identifier: CA355472419

Gene: DNAJC19

Linked Data

• MyVariant Identifiers: chr3:g.180704741G>C (hg19) ; chr3:g.180986953G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180986953G>C , CM000665.2:g.180986953G>C	GRCh38
NC_000003.11:g.180704741G>C , CM000665.1:g.180704741G>C	GRCh37
NC_000003.10:g.182187435G>C	NCBI36
NG_022933.1:g.7822C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.270C>G
ENST00000482363.2:n.1366C>G
ENST00000485675.2:n.1360C>G
ENST00000688055.1:c.199C>G	ENSP00000508688.1:p.Leu67Val
ENST00000382564.8:c.199C>G MANE Select	ENSP00000372005.2:p.Leu67Val
ENST00000643241.1:c.124C>G	ENSP00000496401.1:p.Leu42Val
ENST00000646965.1:c.-46-957C>G	ENSP00000496456.1:n.-46-957C>G
ENST00000382564.6:c.199C>G	ENSP00000372005.2:p.Leu67Val
ENST00000469657.5:c.130-957C>G	ENSP00000418058.1:n.130-957C>G
ENST00000478723.5:n.338C>G
ENST00000479269.5:c.124C>G	ENSP00000419191.1:p.Leu42Val
ENST00000485675.1:n.1272C>G
ENST00000486355.1:c.154+45C>G	ENSP00000419991.1:n.154+45C>G
ENST00000491873.5:c.124C>G	ENSP00000420767.1:p.Leu42Val
NM_001190233.1:c.124C>G	NP_001177162.1:p.Leu42Val
NM_145261.3:c.199C>G	NP_660304.1:p.Leu67Val
NR_033721.1:n.319C>G
NR_033722.1:n.302-957C>G
NR_033723.1:n.326+45C>G
NR_046073.1:n.176-957C>G
NM_145261.4:c.199C>G MANE Select	NP_660304.1:p.Leu67Val
NM_001190233.2:c.124C>G	NP_001177162.1:p.Leu42Val
NR_033721.2:n.281C>G
NR_033722.2:n.264-957C>G