Canonical Allele Identifier: CA437196501

Gene: DNAJC19

Linked Data

• MyVariant Identifiers: chr3:g.180704733T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180986945T>G , CM000665.2:g.180986945T>G	GRCh38
NC_000003.11:g.180704733T>G , CM000665.1:g.180704733T>G	GRCh37
NC_000003.10:g.182187427T>G	NCBI36
NG_022933.1:g.7830A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.278A>C
ENST00000482363.2:n.1374A>C
ENST00000485675.2:n.1368A>C
ENST00000688055.1:c.207A>C	ENSP00000508688.1:p.Val69=
ENST00000382564.8:c.207A>C MANE Select	ENSP00000372005.2:p.Val69=
ENST00000643241.1:c.129+3A>C	ENSP00000496401.1:n.129+3A>C
ENST00000646965.1:c.-46-949A>C	ENSP00000496456.1:n.-46-949A>C
ENST00000382564.6:c.207A>C	ENSP00000372005.2:p.Val69=
ENST00000469657.5:c.130-949A>C	ENSP00000418058.1:n.130-949A>C
ENST00000478723.5:n.346A>C
ENST00000479269.5:c.132A>C	ENSP00000419191.1:p.Val44=
ENST00000485675.1:n.1280A>C
ENST00000486355.1:c.154+53A>C	ENSP00000419991.1:n.154+53A>C
ENST00000491873.5:c.132A>C	ENSP00000420767.1:p.Val44=
NM_001190233.1:c.132A>C	NP_001177162.1:p.Val44=
NM_145261.3:c.207A>C	NP_660304.1:p.Val69=
NR_033721.1:n.327A>C
NR_033722.1:n.302-949A>C
NR_033723.1:n.326+53A>C
NR_046073.1:n.176-949A>C
NM_145261.4:c.207A>C MANE Select	NP_660304.1:p.Val69=
NM_001190233.2:c.132A>C	NP_001177162.1:p.Val44=
NR_033721.2:n.289A>C
NR_033722.2:n.264-949A>C