Canonical Allele Identifier: CA355472481

Gene: DNAJC19

Linked Data

• gnomAD v4: 3-180986981-T-G
• MyVariant Identifiers: chr3:g.180704769T>G (hg19) ; chr3:g.180986981T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180986981T>G , CM000665.2:g.180986981T>G	GRCh38
NC_000003.11:g.180704769T>G , CM000665.1:g.180704769T>G	GRCh37
NC_000003.10:g.182187463T>G	NCBI36
NG_022933.1:g.7794A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478723.6:n.242A>C
ENST00000482363.2:n.1338A>C
ENST00000485675.2:n.1332A>C
ENST00000688055.1:c.171A>C	ENSP00000508688.1:p.Lys57Asn
ENST00000382564.8:c.171A>C MANE Select	ENSP00000372005.2:p.Lys57Asn
ENST00000643241.1:c.96A>C	ENSP00000496401.1:p.Lys32Asn
ENST00000646965.1:c.-46-985A>C	ENSP00000496456.1:n.-46-985A>C
ENST00000382564.6:c.171A>C	ENSP00000372005.2:p.Lys57Asn
ENST00000469657.5:c.130-985A>C	ENSP00000418058.1:n.130-985A>C
ENST00000478723.5:n.310A>C
ENST00000479269.5:c.96A>C	ENSP00000419191.1:p.Lys32Asn
ENST00000485675.1:n.1244A>C
ENST00000486355.1:c.154+17A>C	ENSP00000419991.1:n.154+17A>C
ENST00000491873.5:c.96A>C	ENSP00000420767.1:p.Lys32Asn
NM_001190233.1:c.96A>C	NP_001177162.1:p.Lys32Asn
NM_145261.3:c.171A>C	NP_660304.1:p.Lys57Asn
NR_033721.1:n.291A>C
NR_033722.1:n.302-985A>C
NR_033723.1:n.326+17A>C
NR_046073.1:n.176-985A>C
NM_145261.4:c.171A>C MANE Select	NP_660304.1:p.Lys57Asn
NM_001190233.2:c.96A>C	NP_001177162.1:p.Lys32Asn
NR_033721.2:n.253A>C
NR_033722.2:n.264-985A>C