Canonical Allele Identifier: CA437196799

Gene: DNAJC19

Linked Data

• MyVariant Identifiers: chr3:g.180704802A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180987014A>G , CM000665.2:g.180987014A>G	GRCh38
NC_000003.11:g.180704802A>G , CM000665.1:g.180704802A>G	GRCh37
NC_000003.10:g.182187496A>G	NCBI36
NG_022933.1:g.7761T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.209T>C
ENST00000482363.2:n.1305T>C
ENST00000485675.2:n.1299T>C
ENST00000688055.1:c.138T>C	ENSP00000508688.1:p.Ser46=
ENST00000382564.8:c.138T>C MANE Select	ENSP00000372005.2:p.Ser46=
ENST00000643241.1:c.63T>C	ENSP00000496401.1:p.Ser21=
ENST00000646965.1:c.-46-1018T>C	ENSP00000496456.1:n.-46-1018T>C
ENST00000382564.6:c.138T>C	ENSP00000372005.2:p.Ser46=
ENST00000469657.5:c.129+1009T>C	ENSP00000418058.1:n.129+1009T>C
ENST00000478723.5:n.277T>C
ENST00000479269.5:c.63T>C	ENSP00000419191.1:p.Ser21=
ENST00000485675.1:n.1211T>C
ENST00000486355.1:c.138T>C	ENSP00000419991.1:p.Ser46=
ENST00000491873.5:c.63T>C	ENSP00000420767.1:p.Ser21=
NM_001190233.1:c.63T>C	NP_001177162.1:p.Ser21=
NM_145261.3:c.138T>C	NP_660304.1:p.Ser46=
NR_033721.1:n.258T>C
NR_033722.1:n.301+1009T>C
NR_033723.1:n.310T>C
NR_046073.1:n.176-1018T>C
NM_145261.4:c.138T>C MANE Select	NP_660304.1:p.Ser46=
NM_001190233.2:c.63T>C	NP_001177162.1:p.Ser21=
NR_033721.2:n.220T>C
NR_033722.2:n.263+1009T>C