Canonical Allele Identifier: CA2573139556

Gene: DNAJC21

Linked Data

• ClinVar Variation Id: 1354212
• ClinVar RCV Id: RCV001866308
• dbSNP Id: rs2112004957

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34929854_34929855delinsAG , CM000667.2:g.34929854_34929855delinsAG	GRCh38
NC_000005.9:g.34929959_34929960delinsAG , CM000667.1:g.34929959_34929960delinsAG	GRCh37
NC_000005.8:g.34965716_34965717delinsAG	NCBI36
NG_052822.1:g.5315_5316delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506762.2:c.-314_-313delinsAG	ENSP00000513864.1:n.-314_-313delinsAG
ENST00000512136.2:n.262_263delinsAG
ENST00000642851.1:c.35_36delinsAG	ENSP00000496545.1:p.Arg12Gln
ENST00000648817.1:c.35_36delinsAG MANE Select	ENSP00000497410.1:p.Arg12Gln
ENST00000342382.8:c.35_36delinsAG	ENSP00000343728.4:p.Arg12Gln
ENST00000382021.2:c.35_36delinsAG	ENSP00000371451.2:p.Arg12Gln
NM_001012339.2:c.35_36delinsAG	NP_001012339.2:p.Arg12Gln
NM_194283.3:c.35_36delinsAG	NP_919259.3:p.Arg12Gln
XM_005248249.3:c.35_36delinsAG	XP_005248306.1:p.Arg12Gln
XM_005248250.2:c.35_36delinsAG	XP_005248307.1:p.Arg12Gln
XM_011513965.1:c.35_36delinsAG	XP_011512267.1:p.Arg12Gln
XM_011513966.1:c.35_36delinsAG	XP_011512268.1:p.Arg12Gln
NM_001012339.3:c.35_36delinsAG MANE Select	NP_001012339.2:p.Arg12Gln
NM_001348420.1:c.35_36delinsAG	NP_001335349.1:p.Arg12Gln
XM_005248250.3:c.296_297delinsAG	XP_005248307.2:p.Arg99Gln
XM_011513965.2:c.296_297delinsAG	XP_011512267.2:p.Arg99Gln
XM_011513966.2:c.296_297delinsAG	XP_011512268.2:p.Arg99Gln
NM_001348420.2:c.35_36delinsAG	NP_001335349.1:p.Arg12Gln
NM_194283.4:c.35_36delinsAG	NP_919259.3:p.Arg12Gln