Canonical Allele Identifier: CA2623305213

Gene: CLN5 FBXL3

Linked Data

• gnomAD v4: 13-77001210-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.77001210T>C , CM000675.2:g.77001210T>C	GRCh38
NC_000013.10:g.77575345T>C , CM000675.1:g.77575345T>C	GRCh37
NC_000013.9:g.76473346T>C	NCBI36
NG_009064.1:g.14287T>C , LRG_692:g.14287T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377453.9:c.*241T>C (CLN5) MANE Select	ENSP00000366673.5:n.*241T>C
ENST00000616833.6:c.*760T>C (CLN5)	ENSP00000479547.3:n.*760T>C
ENST00000635838.1:c.174+5083T>C
ENST00000635905.1:n.566+5083T>C (CLN5)
ENST00000635915.1:c.1316T>C (CLN5)
ENST00000636183.2:c.*241T>C (CLN5)	ENSP00000490181.2:n.*241T>C
ENST00000636525.2:c.565+5083T>C (CLN5)	ENSP00000490078.2:n.565+5083T>C
ENST00000636681.1:c.*1009T>C (CLN5)	ENSP00000489922.1:n.*1009T>C
ENST00000636705.1:c.1154T>C (CLN5)
ENST00000636767.2:c.565+5083T>C (CLN5)	ENSP00000489855.2:n.565+5083T>C
ENST00000636780.2:c.*767T>C (CLN5)	ENSP00000489809.2:n.*767T>C
ENST00000637192.1:c.213+5083T>C
ENST00000637278.1:n.1644T>C (CLN5)
ENST00000637397.2:c.565+5083T>C (CLN5)	ENSP00000490422.2:n.565+5083T>C
ENST00000638101.1:c.169+5083T>C	ENSP00000490535.1:n.169+5083T>C
ENST00000638147.2:c.565+5083T>C	ENSP00000490953.2:n.565+5083T>C
ENST00000377453.7:c.*241T>C (CLN5)	ENSP00000366673.3:n.*241T>C
ENST00000477982.2:n.1099A>G (FBXL3)
ENST00000485797.2:n.174-8259A>G (FBXL3)
ENST00000616833.4:c.*241T>C (CLN5)	ENSP00000479547.1:n.*241T>C
NM_006493.2:c.*241T>C , LRG_692t1:c.*241T>C (CLN5)	NP_006484.1:n.*241T>C
NM_001366624.1:c.*767T>C (CLN5)	NP_001353553.1:n.*767T>C
NM_006493.3:c.*241T>C (CLN5)	NP_006484.2:n.*241T>C
XM_017020538.2:c.644-8259A>G (FBXL3)	XP_016876027.1:n.644-8259A>G
NM_001366624.2:c.*767T>C (CLN5)	NP_001353553.1:n.*767T>C
NM_006493.4:c.*241T>C (CLN5) MANE Select	NP_006484.2:n.*241T>C