Canonical Allele Identifier: CA11926170

Gene: DNAJC21

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34951045C>A , CM000667.2:g.34951045C>A	GRCh38
NC_000005.9:g.34951150C>A , CM000667.1:g.34951150C>A	GRCh37
NC_000005.8:g.34986907C>A	NCBI36
NG_052822.1:g.26506C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000506762.2:c.1010+703C>A	ENSP00000513864.1:n.1010+703C>A
ENST00000512136.2:n.2187C>A
ENST00000644357.2:c.1145+703C>A	ENSP00000493850.2:n.1145+703C>A
ENST00000698659.1:n.803+703C>A
ENST00000698660.1:n.2143+703C>A
ENST00000698661.1:n.2383+703C>A
ENST00000642285.1:c.1184+703C>A	ENSP00000493883.1:n.1184+703C>A
ENST00000642675.1:c.1010+703C>A	ENSP00000494173.1:n.1010+703C>A
ENST00000642851.1:c.1397+703C>A	ENSP00000496545.1:n.1397+703C>A
ENST00000646714.1:c.*775+703C>A	ENSP00000495883.1:n.*775+703C>A
ENST00000648817.1:c.1358+703C>A MANE Select	ENSP00000497410.1:n.1358+703C>A
ENST00000342382.8:c.1358+703C>A	ENSP00000343728.4:n.1358+703C>A
ENST00000382021.2:c.1493+703C>A	ENSP00000371451.2:n.1493+703C>A
ENST00000506762.1:n.136+703C>A
ENST00000512136.1:n.818C>A
ENST00000514237.5:n.1022+703C>A
NM_001012339.2:c.1358+703C>A	NP_001012339.2:n.1358+703C>A
NM_194283.3:c.1493+703C>A	NP_919259.3:n.1493+703C>A
XM_005248249.3:c.1397+703C>A	XP_005248306.1:n.1397+703C>A
XM_005248250.2:c.*598C>A	XP_005248307.1:n.*598C>A
XM_011513965.1:c.1532+703C>A	XP_011512267.1:n.1532+703C>A
XM_011513966.1:c.*598C>A	XP_011512268.1:n.*598C>A
NM_001012339.3:c.1358+703C>A MANE Select	NP_001012339.2:n.1358+703C>A
NM_001348420.1:c.1397+703C>A	NP_001335349.1:n.1397+703C>A
XM_005248250.3:c.*598C>A	XP_005248307.2:n.*598C>A
XM_011513965.2:c.1793+703C>A	XP_011512267.2:n.1793+703C>A
XM_011513966.2:c.*598C>A	XP_011512268.2:n.*598C>A
NM_001348420.2:c.1397+703C>A	NP_001335349.1:n.1397+703C>A
NM_194283.4:c.1493+703C>A	NP_919259.3:n.1493+703C>A