Canonical Allele Identifier: CA355472546

Gene: DNAJC19

Linked Data

• MyVariant Identifiers: chr3:g.180704797C>G (hg19) ; chr3:g.180987009C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180987009C>G , CM000665.2:g.180987009C>G	GRCh38
NC_000003.11:g.180704797C>G , CM000665.1:g.180704797C>G	GRCh37
NC_000003.10:g.182187491C>G	NCBI36
NG_022933.1:g.7766G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.214G>C
ENST00000482363.2:n.1310G>C
ENST00000485675.2:n.1304G>C
ENST00000688055.1:c.143G>C	ENSP00000508688.1:p.Gly48Ala
ENST00000382564.8:c.143G>C MANE Select	ENSP00000372005.2:p.Gly48Ala
ENST00000643241.1:c.68G>C	ENSP00000496401.1:p.Gly23Ala
ENST00000646965.1:c.-46-1013G>C	ENSP00000496456.1:n.-46-1013G>C
ENST00000382564.6:c.143G>C	ENSP00000372005.2:p.Gly48Ala
ENST00000469657.5:c.130-1013G>C	ENSP00000418058.1:n.130-1013G>C
ENST00000478723.5:n.282G>C
ENST00000479269.5:c.68G>C	ENSP00000419191.1:p.Gly23Ala
ENST00000485675.1:n.1216G>C
ENST00000486355.1:c.143G>C	ENSP00000419991.1:p.Gly48Ala
ENST00000491873.5:c.68G>C	ENSP00000420767.1:p.Gly23Ala
NM_001190233.1:c.68G>C	NP_001177162.1:p.Gly23Ala
NM_145261.3:c.143G>C	NP_660304.1:p.Gly48Ala
NR_033721.1:n.263G>C
NR_033722.1:n.302-1013G>C
NR_033723.1:n.315G>C
NR_046073.1:n.176-1013G>C
NM_145261.4:c.143G>C MANE Select	NP_660304.1:p.Gly48Ala
NM_001190233.2:c.68G>C	NP_001177162.1:p.Gly23Ala
NR_033721.2:n.225G>C
NR_033722.2:n.264-1013G>C