Canonical Allele Identifier: CA1538654585

Gene: DNAJC21

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34935822G= , CM000667.2:g.34935822G=	GRCh38
NC_000005.9:g.34935927G= , CM000667.1:g.34935927G=	GRCh37
NC_000005.8:g.34971684G=	NCBI36
NG_052822.1:g.11283G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506762.2:c.-45G=	ENSP00000513864.1:n.-45G=
ENST00000512136.2:n.531G=
ENST00000644357.2:c.-45G=	ENSP00000493850.2:n.-45G=
ENST00000698657.1:n.462G=
ENST00000698658.1:n.462G=
ENST00000642285.1:c.-45G=	ENSP00000493883.1:n.-45G=
ENST00000642675.1:c.-45G=	ENSP00000494173.1:n.-45G=
ENST00000642851.1:c.304G=	ENSP00000496545.1:p.Asp102=
ENST00000644357.1:c.-45G=	ENSP00000493850.1:n.-45G=
ENST00000646714.1:c.-45G=	ENSP00000495883.1:n.-45G=
ENST00000648817.1:c.304G= MANE Select	ENSP00000497410.1:p.Asp102=
ENST00000342382.8:c.304G=	ENSP00000343728.4:p.Asp102=
ENST00000382021.2:c.304G=	ENSP00000371451.2:p.Asp102=
NM_001012339.2:c.304G=	NP_001012339.2:p.Asp102=
NM_194283.3:c.304G=	NP_919259.3:p.Asp102=
XM_005248249.3:c.304G=	XP_005248306.1:p.Asp102=
XM_005248250.2:c.304G=	XP_005248307.1:p.Asp102=
XM_011513965.1:c.304G=	XP_011512267.1:p.Asp102=
XM_011513966.1:c.304G=	XP_011512268.1:p.Asp102=
NM_001012339.3:c.304G= MANE Select	NP_001012339.2:p.Asp102=
NM_001348420.1:c.304G=	NP_001335349.1:p.Asp102=
XM_005248250.3:c.565G=	XP_005248307.2:p.Asp189=
XM_011513965.2:c.565G=	XP_011512267.2:p.Asp189=
XM_011513966.2:c.565G=	XP_011512268.2:p.Asp189=
NM_001348420.2:c.304G=	NP_001335349.1:p.Asp102=
NM_194283.4:c.304G=	NP_919259.3:p.Asp102=