Canonical Allele Identifier: CA2765859812

Gene: DNAJC21

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34935938_34935939insAGATCTCGGAGATCGCCGTA , CM000667.2:g.34935938_34935939insAGATCTCGGAGATCGCCGTA	GRCh38
NC_000005.9:g.34936043_34936044insAGATCTCGGAGATCGCCGTA , CM000667.1:g.34936043_34936044insAGATCTCGGAGATCGCCGTA	GRCh37
NC_000005.8:g.34971800_34971801insAGATCTCGGAGATCGCCGTA	NCBI36
NG_052822.1:g.11399_11400insAGATCTCGGAGATCGCCGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506762.2:c.-34+105_-34+106insAGATCTCGGAGATCGCCGTA	ENSP00000513864.1:n.-34+105_-34+106insAGATCTCGGAGATCGCCGTA
ENST00000512136.2:n.542+105_542+106insAGATCTCGGAGATCGCCGTA
ENST00000644357.2:c.-34+105_-34+106insAGATCTCGGAGATCGCCGTA	ENSP00000493850.2:n.-34+105_-34+106insAGATCTCGGAGATCGCCGTA
ENST00000698657.1:n.473+105_473+106insAGATCTCGGAGATCGCCGTA
ENST00000698658.1:n.473+105_473+106insAGATCTCGGAGATCGCCGTA
ENST00000642285.1:c.-34+105_-34+106insAGATCTCGGAGATCGCCGTA	ENSP00000493883.1:n.-34+105_-34+106insAGATCTCGGAGATCGCCGTA
ENST00000642675.1:c.-34+105_-34+106insAGATCTCGGAGATCGCCGTA	ENSP00000494173.1:n.-34+105_-34+106insAGATCTCGGAGATCGCCGTA
ENST00000642851.1:c.315+105_315+106insAGATCTCGGAGATCGCCGTA	ENSP00000496545.1:n.315+105_315+106insAGATCTCGGAGATCGCCGTA
ENST00000644357.1:c.-34+105_-34+106insAGATCTCGGAGATCGCCGTA	ENSP00000493850.1:n.-34+105_-34+106insAGATCTCGGAGATCGCCGTA
ENST00000646714.1:c.-34+105_-34+106insAGATCTCGGAGATCGCCGTA	ENSP00000495883.1:n.-34+105_-34+106insAGATCTCGGAGATCGCCGTA
ENST00000648817.1:c.315+105_315+106insAGATCTCGGAGATCGCCGTA MANE Select	ENSP00000497410.1:n.315+105_315+106insAGATCTCGGAGATCGCCGTA
ENST00000342382.8:c.315+105_315+106insAGATCTCGGAGATCGCCGTA	ENSP00000343728.4:n.315+105_315+106insAGATCTCGGAGATCGCCGTA
ENST00000382021.2:c.315+105_315+106insAGATCTCGGAGATCGCCGTA	ENSP00000371451.2:n.315+105_315+106insAGATCTCGGAGATCGCCGTA
NM_001012339.2:c.315+105_315+106insAGATCTCGGAGATCGCCGTA	NP_001012339.2:n.315+105_315+106insAGATCTCGGAGATCGCCGTA
NM_194283.3:c.315+105_315+106insAGATCTCGGAGATCGCCGTA	NP_919259.3:n.315+105_315+106insAGATCTCGGAGATCGCCGTA
XM_005248249.3:c.315+105_315+106insAGATCTCGGAGATCGCCGTA	XP_005248306.1:n.315+105_315+106insAGATCTCGGAGATCGCCGTA
XM_005248250.2:c.315+105_315+106insAGATCTCGGAGATCGCCGTA	XP_005248307.1:n.315+105_315+106insAGATCTCGGAGATCGCCGTA
XM_011513965.1:c.315+105_315+106insAGATCTCGGAGATCGCCGTA	XP_011512267.1:n.315+105_315+106insAGATCTCGGAGATCGCCGTA
XM_011513966.1:c.315+105_315+106insAGATCTCGGAGATCGCCGTA	XP_011512268.1:n.315+105_315+106insAGATCTCGGAGATCGCCGTA
NM_001012339.3:c.315+105_315+106insAGATCTCGGAGATCGCCGTA MANE Select	NP_001012339.2:n.315+105_315+106insAGATCTCGGAGATCGCCGTA
NM_001348420.1:c.315+105_315+106insAGATCTCGGAGATCGCCGTA	NP_001335349.1:n.315+105_315+106insAGATCTCGGAGATCGCCGTA
XM_005248250.3:c.576+105_576+106insAGATCTCGGAGATCGCCGTA	XP_005248307.2:n.576+105_576+106insAGATCTCGGAGATCGCCGTA
XM_011513965.2:c.576+105_576+106insAGATCTCGGAGATCGCCGTA	XP_011512267.2:n.576+105_576+106insAGATCTCGGAGATCGCCGTA
XM_011513966.2:c.576+105_576+106insAGATCTCGGAGATCGCCGTA	XP_011512268.2:n.576+105_576+106insAGATCTCGGAGATCGCCGTA
NM_001348420.2:c.315+105_315+106insAGATCTCGGAGATCGCCGTA	NP_001335349.1:n.315+105_315+106insAGATCTCGGAGATCGCCGTA
NM_194283.4:c.315+105_315+106insAGATCTCGGAGATCGCCGTA	NP_919259.3:n.315+105_315+106insAGATCTCGGAGATCGCCGTA