Canonical Allele Identifier: CA2103434548

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.77000309_77000312delinsCAGG , CM000675.2:g.77000309_77000312delinsCAGG GRCh38
NC_000013.10:g.77574444_77574447delinsCAGG , CM000675.1:g.77574444_77574447delinsCAGG GRCh37
NC_000013.9:g.76472445_76472448delinsCAGG NCBI36
NG_009064.1:g.13386_13389delinsCAGG , LRG_692:g.13386_13389delinsCAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000377453.9:c.566-149_566-146delinsCAGG (CLN5) MANE Select ENSP00000366673.5:n.566-149_566-146delinsCAGG
ENST00000616833.6:c.*8-149_*8-146delinsCAGG (CLN5) ENSP00000479547.3:n.*8-149_*8-146delinsCAGG
ENST00000635761.1:n.475_478delinsCAGG (CLN5)
ENST00000635838.1:c.174+4182_174+4185delinsCAGG
ENST00000635905.1:n.566+4182_566+4185delinsCAGG (CLN5)
ENST00000635915.1:c.564-149_564-146delinsCAGG (CLN5)
ENST00000636183.2:c.566-149_566-146delinsCAGG (CLN5) ENSP00000490181.2:n.566-149_566-146delinsCAGG
ENST00000636525.2:c.565+4182_565+4185delinsCAGG (CLN5) ENSP00000490078.2:n.565+4182_565+4185delinsCAGG
ENST00000636681.1:c.*257-149_*257-146delinsCAGG (CLN5) ENSP00000489922.1:n.*257-149_*257-146delinsCAGG
ENST00000636705.1:c.402-149_402-146delinsCAGG (CLN5)
ENST00000636767.2:c.565+4182_565+4185delinsCAGG (CLN5) ENSP00000489855.2:n.565+4182_565+4185delinsCAGG
ENST00000636780.2:c.*15-149_*15-146delinsCAGG (CLN5) ENSP00000489809.2:n.*15-149_*15-146delinsCAGG
ENST00000637192.1:c.213+4182_213+4185delinsCAGG
ENST00000637278.1:n.892-149_892-146delinsCAGG (CLN5)
ENST00000637397.2:c.565+4182_565+4185delinsCAGG (CLN5) ENSP00000490422.2:n.565+4182_565+4185delinsCAGG
ENST00000638101.1:c.169+4182_169+4185delinsCAGG ENSP00000490535.1:n.169+4182_169+4185delinsCAGG
ENST00000638147.2:c.565+4182_565+4185delinsCAGG ENSP00000490953.2:n.565+4182_565+4185delinsCAGG
ENST00000377453.7:c.713-149_713-146delinsCAGG (CLN5) ENSP00000366673.3:n.713-149_713-146delinsCAGG
ENST00000477982.2:n.1997_2000delinsCCTG (FBXL3)
ENST00000485797.2:n.174-7361_174-7358delinsCCTG (FBXL3)
ENST00000616833.4:c.566-149_566-146delinsCAGG (CLN5) ENSP00000479547.1:n.566-149_566-146delinsCAGG
NM_006493.2:c.713-149_713-146delinsCAGG , LRG_692t1:c.713-149_713-146delinsCAGG (CLN5) NP_006484.1:n.713-149_713-146delinsCAGG
XM_011534917.1:c.*15-149_*15-146delinsCAGG (CLN5) XP_011533219.1:n.*15-149_*15-146delinsCAGG
NM_001366624.1:c.*15-149_*15-146delinsCAGG (CLN5) NP_001353553.1:n.*15-149_*15-146delinsCAGG
NM_006493.3:c.566-149_566-146delinsCAGG (CLN5) NP_006484.2:n.566-149_566-146delinsCAGG
XM_017020538.2:c.644-7361_644-7358delinsCCTG (FBXL3) XP_016876027.1:n.644-7361_644-7358delinsCCTG
NM_001366624.2:c.*15-149_*15-146delinsCAGG (CLN5) NP_001353553.1:n.*15-149_*15-146delinsCAGG
NM_006493.4:c.566-149_566-146delinsCAGG (CLN5) MANE Select NP_006484.2:n.566-149_566-146delinsCAGG