Canonical Allele Identifier: CA443884820

Gene: DNAJC21

Linked Data

• MyVariant Identifiers: chr5:g.34935920T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34935815T>A , CM000667.2:g.34935815T>A	GRCh38
NC_000005.9:g.34935920T>A , CM000667.1:g.34935920T>A	GRCh37
NC_000005.8:g.34971677T>A	NCBI36
NG_052822.1:g.11276T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506762.2:c.-52T>A	ENSP00000513864.1:n.-52T>A
ENST00000512136.2:n.524T>A
ENST00000644357.2:c.-52T>A	ENSP00000493850.2:n.-52T>A
ENST00000698657.1:n.455T>A
ENST00000698658.1:n.455T>A
ENST00000642285.1:c.-52T>A	ENSP00000493883.1:n.-52T>A
ENST00000642675.1:c.-52T>A	ENSP00000494173.1:n.-52T>A
ENST00000642851.1:c.297T>A	ENSP00000496545.1:p.Gly99=
ENST00000644357.1:c.-52T>A	ENSP00000493850.1:n.-52T>A
ENST00000646714.1:c.-52T>A	ENSP00000495883.1:n.-52T>A
ENST00000648817.1:c.297T>A MANE Select	ENSP00000497410.1:p.Gly99=
ENST00000342382.8:c.297T>A	ENSP00000343728.4:p.Gly99=
ENST00000382021.2:c.297T>A	ENSP00000371451.2:p.Gly99=
NM_001012339.2:c.297T>A	NP_001012339.2:p.Gly99=
NM_194283.3:c.297T>A	NP_919259.3:p.Gly99=
XM_005248249.3:c.297T>A	XP_005248306.1:p.Gly99=
XM_005248250.2:c.297T>A	XP_005248307.1:p.Gly99=
XM_011513965.1:c.297T>A	XP_011512267.1:p.Gly99=
XM_011513966.1:c.297T>A	XP_011512268.1:p.Gly99=
NM_001012339.3:c.297T>A MANE Select	NP_001012339.2:p.Gly99=
NM_001348420.1:c.297T>A	NP_001335349.1:p.Gly99=
XM_005248250.3:c.558T>A	XP_005248307.2:p.Gly186=
XM_011513965.2:c.558T>A	XP_011512267.2:p.Gly186=
XM_011513966.2:c.558T>A	XP_011512268.2:p.Gly186=
NM_001348420.2:c.297T>A	NP_001335349.1:p.Gly99=
NM_194283.4:c.297T>A	NP_919259.3:p.Gly99=