Canonical Allele Identifier: CA388313963

Gene: CLN5 FBXL3

Linked Data

• dbSNP Id: rs1463859201
• gnomAD v2: 13-77574907-C-T
• gnomAD v4: 13-77000772-C-T
• MyVariant Identifiers: chr13:g.77574907C>T (hg19) ; chr13:g.77000772C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.77000772C>T , CM000675.2:g.77000772C>T	GRCh38
NC_000013.10:g.77574907C>T , CM000675.1:g.77574907C>T	GRCh37
NC_000013.9:g.76472908C>T	NCBI36
NG_009064.1:g.13849C>T , LRG_692:g.13849C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000377453.9:c.880C>T (CLN5) MANE Select	ENSP00000366673.5:p.Pro294Ser
ENST00000616833.6:c.*322C>T (CLN5)	ENSP00000479547.3:n.*322C>T
ENST00000635838.1:c.174+4645C>T
ENST00000635905.1:n.566+4645C>T (CLN5)
ENST00000635915.1:c.878C>T (CLN5)
ENST00000636183.2:c.880C>T (CLN5)	ENSP00000490181.2:p.Pro294Ser
ENST00000636525.2:c.565+4645C>T (CLN5)	ENSP00000490078.2:n.565+4645C>T
ENST00000636681.1:c.*571C>T (CLN5)	ENSP00000489922.1:n.*571C>T
ENST00000636705.1:c.716C>T (CLN5)
ENST00000636767.2:c.565+4645C>T (CLN5)	ENSP00000489855.2:n.565+4645C>T
ENST00000636780.2:c.*329C>T (CLN5)	ENSP00000489809.2:n.*329C>T
ENST00000637192.1:c.213+4645C>T
ENST00000637278.1:n.1206C>T (CLN5)
ENST00000637397.2:c.565+4645C>T (CLN5)	ENSP00000490422.2:n.565+4645C>T
ENST00000638101.1:c.169+4645C>T	ENSP00000490535.1:n.169+4645C>T
ENST00000638147.2:c.565+4645C>T	ENSP00000490953.2:n.565+4645C>T
ENST00000377453.7:c.1027C>T (CLN5)	ENSP00000366673.3:p.Pro343Ser
ENST00000477982.2:n.1537G>A (FBXL3)
ENST00000485797.2:n.174-7821G>A (FBXL3)
ENST00000616833.4:c.880C>T (CLN5)	ENSP00000479547.1:p.Pro294Ser
NM_006493.2:c.1027C>T , LRG_692t1:c.1027C>T (CLN5)	NP_006484.1:p.Pro343Ser
XM_011534917.1:c.*329C>T (CLN5)	XP_011533219.1:n.*329C>T
NM_001366624.1:c.*329C>T (CLN5)	NP_001353553.1:n.*329C>T
NM_006493.3:c.880C>T (CLN5)	NP_006484.2:p.Pro294Ser
XM_017020538.2:c.644-7821G>A (FBXL3)	XP_016876027.1:n.644-7821G>A
NM_001366624.2:c.*329C>T (CLN5)	NP_001353553.1:n.*329C>T
NM_006493.4:c.880C>T (CLN5) MANE Select	NP_006484.2:p.Pro294Ser