Canonical Allele Identifier: CA1538654448
Gene: DNAJC21 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.34935741G= , CM000667.2:g.34935741G= GRCh38
NC_000005.9:g.34935846G= , CM000667.1:g.34935846G= GRCh37
NC_000005.8:g.34971603G= NCBI36
NG_052822.1:g.11202G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000506762.2:c.-126G= ENSP00000513864.1:n.-126G=
ENST00000512136.2:n.450G=
ENST00000644357.2:c.-126G= ENSP00000493850.2:n.-126G=
ENST00000698657.1:n.381G=
ENST00000698658.1:n.381G=
ENST00000642285.1:c.-126G= ENSP00000493883.1:n.-126G=
ENST00000642675.1:c.-126G= ENSP00000494173.1:n.-126G=
ENST00000642851.1:c.223G= ENSP00000496545.1:p.Gly75=
ENST00000644357.1:c.-126G= ENSP00000493850.1:n.-126G=
ENST00000646714.1:c.-126G= ENSP00000495883.1:n.-126G=
ENST00000648817.1:c.223G= MANE Select ENSP00000497410.1:p.Gly75=
ENST00000342382.8:c.223G= ENSP00000343728.4:p.Gly75=
ENST00000382021.2:c.223G= ENSP00000371451.2:p.Gly75=
NM_001012339.2:c.223G= NP_001012339.2:p.Gly75=
NM_194283.3:c.223G= NP_919259.3:p.Gly75=
XM_005248249.3:c.223G= XP_005248306.1:p.Gly75=
XM_005248250.2:c.223G= XP_005248307.1:p.Gly75=
XM_011513965.1:c.223G= XP_011512267.1:p.Gly75=
XM_011513966.1:c.223G= XP_011512268.1:p.Gly75=
NM_001012339.3:c.223G= MANE Select NP_001012339.2:p.Gly75=
NM_001348420.1:c.223G= NP_001335349.1:p.Gly75=
XM_005248250.3:c.484G= XP_005248307.2:p.Gly162=
XM_011513965.2:c.484G= XP_011512267.2:p.Gly162=
XM_011513966.2:c.484G= XP_011512268.2:p.Gly162=
NM_001348420.2:c.223G= NP_001335349.1:p.Gly75=
NM_194283.4:c.223G= NP_919259.3:p.Gly75=