Canonical Allele Identifier: CA3228373

Gene: DNAJC21

Linked Data

• ClinVar Variation Id: 2419259
• ClinVar RCV Id: RCV003112503
• dbSNP Id: rs753708158
• ExAC: 5:34935821 T / C
• gnomAD v2: 5-34935821-T-C
• gnomAD v3: 5-34935716-T-C
• gnomAD v4: 5-34935716-T-C
• MyVariant Identifiers: chr5:g.34935821T>C (hg19) ; chr5:g.34935716T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34935716T>C , CM000667.2:g.34935716T>C	GRCh38
NC_000005.9:g.34935821T>C , CM000667.1:g.34935821T>C	GRCh37
NC_000005.8:g.34971578T>C	NCBI36
NG_052822.1:g.11177T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506762.2:c.-151T>C	ENSP00000513864.1:n.-151T>C
ENST00000512136.2:n.425T>C
ENST00000644357.2:c.-151T>C	ENSP00000493850.2:n.-151T>C
ENST00000698657.1:n.356T>C
ENST00000698658.1:n.356T>C
ENST00000642285.1:c.-151T>C	ENSP00000493883.1:n.-151T>C
ENST00000642675.1:c.-151T>C	ENSP00000494173.1:n.-151T>C
ENST00000642851.1:c.198T>C	ENSP00000496545.1:p.Asp66=
ENST00000644357.1:c.-151T>C	ENSP00000493850.1:n.-151T>C
ENST00000646714.1:c.-151T>C	ENSP00000495883.1:n.-151T>C
ENST00000648817.1:c.198T>C MANE Select	ENSP00000497410.1:p.Asp66=
ENST00000342382.8:c.198T>C	ENSP00000343728.4:p.Asp66=
ENST00000382021.2:c.198T>C	ENSP00000371451.2:p.Asp66=
NM_001012339.2:c.198T>C	NP_001012339.2:p.Asp66=
NM_194283.3:c.198T>C	NP_919259.3:p.Asp66=
XM_005248249.3:c.198T>C	XP_005248306.1:p.Asp66=
XM_005248250.2:c.198T>C	XP_005248307.1:p.Asp66=
XM_011513965.1:c.198T>C	XP_011512267.1:p.Asp66=
XM_011513966.1:c.198T>C	XP_011512268.1:p.Asp66=
NM_001012339.3:c.198T>C MANE Select	NP_001012339.2:p.Asp66=
NM_001348420.1:c.198T>C	NP_001335349.1:p.Asp66=
XM_005248250.3:c.459T>C	XP_005248307.2:p.Asp153=
XM_011513965.2:c.459T>C	XP_011512267.2:p.Asp153=
XM_011513966.2:c.459T>C	XP_011512268.2:p.Asp153=
NM_001348420.2:c.198T>C	NP_001335349.1:p.Asp66=
NM_194283.4:c.198T>C	NP_919259.3:p.Asp66=