Canonical Allele Identifier: CA701024192

Gene: CLN5 FBXL3

Linked Data

• dbSNP Id: rs1490800638
• gnomAD v3: 13-76996413-C-T
• gnomAD v4: 13-76996413-C-T
• MyVariant Identifiers: chr13:g.77570548C>T (hg19) ; chr13:g.76996413C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.76996413C>T , CM000675.2:g.76996413C>T	GRCh38
NC_000013.10:g.77570548C>T , CM000675.1:g.77570548C>T	GRCh37
NC_000013.9:g.76468549C>T	NCBI36
NG_009064.1:g.9490C>T , LRG_692:g.9490C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377453.9:c.565+286C>T (CLN5) MANE Select	ENSP00000366673.5:n.565+286C>T
ENST00000485938.4:c.*275C>T (CLN5)	ENSP00000482959.3:n.*275C>T
ENST00000616833.6:c.565+286C>T (CLN5)	ENSP00000479547.3:n.565+286C>T
ENST00000635838.1:c.174+286C>T
ENST00000635905.1:n.566+286C>T (CLN5)
ENST00000635915.1:c.563+286C>T (CLN5)
ENST00000636183.2:c.565+286C>T (CLN5)	ENSP00000490181.2:n.565+286C>T
ENST00000636520.1:n.2363C>T (CLN5)
ENST00000636525.2:c.565+286C>T (CLN5)	ENSP00000490078.2:n.565+286C>T
ENST00000636681.1:c.*256+286C>T (CLN5)	ENSP00000489922.1:n.*256+286C>T
ENST00000636705.1:c.401+286C>T (CLN5)
ENST00000636767.2:c.565+286C>T (CLN5)	ENSP00000489855.2:n.565+286C>T
ENST00000636780.2:c.565+286C>T (CLN5)	ENSP00000489809.2:n.565+286C>T
ENST00000637192.1:c.213+286C>T
ENST00000637278.1:n.891+286C>T (CLN5)
ENST00000637397.2:c.565+286C>T (CLN5)	ENSP00000490422.2:n.565+286C>T
ENST00000637537.2:c.565+286C>T (CLN5)	ENSP00000489711.2:n.565+286C>T
ENST00000638101.1:c.169+286C>T	ENSP00000490535.1:n.169+286C>T
ENST00000638147.2:c.565+286C>T	ENSP00000490953.2:n.565+286C>T
ENST00000377453.7:c.712+286C>T (CLN5)	ENSP00000366673.3:n.712+286C>T
ENST00000485797.2:n.174-3462G>A (FBXL3)
ENST00000616833.4:c.565+286C>T (CLN5)	ENSP00000479547.1:n.565+286C>T
NM_006493.2:c.712+286C>T , LRG_692t1:c.712+286C>T (CLN5)	NP_006484.1:n.712+286C>T
XM_011534917.1:c.712+286C>T (CLN5)	XP_011533219.1:n.712+286C>T
NM_001366624.1:c.565+286C>T (CLN5)	NP_001353553.1:n.565+286C>T
NM_006493.3:c.565+286C>T (CLN5)	NP_006484.2:n.565+286C>T
XM_017020538.2:c.644-3462G>A (FBXL3)	XP_016876027.1:n.644-3462G>A
NM_001366624.2:c.565+286C>T (CLN5)	NP_001353553.1:n.565+286C>T
NM_006493.4:c.565+286C>T (CLN5) MANE Select	NP_006484.2:n.565+286C>T