Canonical Allele Identifier: CA359413399

Gene: DNAJC21

Linked Data

• MyVariant Identifiers: chr5:g.34935919G>T (hg19) ; chr5:g.34935814G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34935814G>T , CM000667.2:g.34935814G>T	GRCh38
NC_000005.9:g.34935919G>T , CM000667.1:g.34935919G>T	GRCh37
NC_000005.8:g.34971676G>T	NCBI36
NG_052822.1:g.11275G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506762.2:c.-53G>T	ENSP00000513864.1:n.-53G>T
ENST00000512136.2:n.523G>T
ENST00000644357.2:c.-53G>T	ENSP00000493850.2:n.-53G>T
ENST00000698657.1:n.454G>T
ENST00000698658.1:n.454G>T
ENST00000642285.1:c.-53G>T	ENSP00000493883.1:n.-53G>T
ENST00000642675.1:c.-53G>T	ENSP00000494173.1:n.-53G>T
ENST00000642851.1:c.296G>T	ENSP00000496545.1:p.Gly99Val
ENST00000644357.1:c.-53G>T	ENSP00000493850.1:n.-53G>T
ENST00000646714.1:c.-53G>T	ENSP00000495883.1:n.-53G>T
ENST00000648817.1:c.296G>T MANE Select	ENSP00000497410.1:p.Gly99Val
ENST00000342382.8:c.296G>T	ENSP00000343728.4:p.Gly99Val
ENST00000382021.2:c.296G>T	ENSP00000371451.2:p.Gly99Val
NM_001012339.2:c.296G>T	NP_001012339.2:p.Gly99Val
NM_194283.3:c.296G>T	NP_919259.3:p.Gly99Val
XM_005248249.3:c.296G>T	XP_005248306.1:p.Gly99Val
XM_005248250.2:c.296G>T	XP_005248307.1:p.Gly99Val
XM_011513965.1:c.296G>T	XP_011512267.1:p.Gly99Val
XM_011513966.1:c.296G>T	XP_011512268.1:p.Gly99Val
NM_001012339.3:c.296G>T MANE Select	NP_001012339.2:p.Gly99Val
NM_001348420.1:c.296G>T	NP_001335349.1:p.Gly99Val
XM_005248250.3:c.557G>T	XP_005248307.2:p.Gly186Val
XM_011513965.2:c.557G>T	XP_011512267.2:p.Gly186Val
XM_011513966.2:c.557G>T	XP_011512268.2:p.Gly186Val
NM_001348420.2:c.296G>T	NP_001335349.1:p.Gly99Val
NM_194283.4:c.296G>T	NP_919259.3:p.Gly99Val