Canonical Allele Identifier: CA2103436578

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.77000882_77000883delinsGT , CM000675.2:g.77000882_77000883delinsGT GRCh38
NC_000013.10:g.77575017_77575018delinsGT , CM000675.1:g.77575017_77575018delinsGT GRCh37
NC_000013.9:g.76473018_76473019delinsGT NCBI36
NG_009064.1:g.13959_13960delinsGT , LRG_692:g.13959_13960delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000377453.9:c.990_991delinsGT (CLN5) MANE Select ENSP00000366673.5:p.Trp330=
ENST00000616833.6:c.*432_*433delinsGT (CLN5) ENSP00000479547.3:n.*432_*433delinsGT
ENST00000635838.1:c.174+4755_174+4756delinsGT
ENST00000635905.1:n.566+4755_566+4756delinsGT (CLN5)
ENST00000635915.1:c.988_989delinsGT (CLN5)
ENST00000636183.2:c.990_991delinsGT (CLN5) ENSP00000490181.2:p.Trp330=
ENST00000636525.2:c.565+4755_565+4756delinsGT (CLN5) ENSP00000490078.2:n.565+4755_565+4756delinsGT
ENST00000636681.1:c.*681_*682delinsGT (CLN5) ENSP00000489922.1:n.*681_*682delinsGT
ENST00000636705.1:c.826_827delinsGT (CLN5)
ENST00000636767.2:c.565+4755_565+4756delinsGT (CLN5) ENSP00000489855.2:n.565+4755_565+4756delinsGT
ENST00000636780.2:c.*439_*440delinsGT (CLN5) ENSP00000489809.2:n.*439_*440delinsGT
ENST00000637192.1:c.213+4755_213+4756delinsGT
ENST00000637278.1:n.1316_1317delinsGT (CLN5)
ENST00000637397.2:c.565+4755_565+4756delinsGT (CLN5) ENSP00000490422.2:n.565+4755_565+4756delinsGT
ENST00000638101.1:c.169+4755_169+4756delinsGT ENSP00000490535.1:n.169+4755_169+4756delinsGT
ENST00000638147.2:c.565+4755_565+4756delinsGT ENSP00000490953.2:n.565+4755_565+4756delinsGT
ENST00000377453.7:c.1137_1138delinsGT (CLN5) ENSP00000366673.3:p.Trp379=
ENST00000477982.2:n.1426_1427delinsAC (FBXL3)
ENST00000485797.2:n.174-7932_174-7931delinsAC (FBXL3)
ENST00000616833.4:c.990_991delinsGT (CLN5) ENSP00000479547.1:p.Trp330=
NM_006493.2:c.1137_1138delinsGT , LRG_692t1:c.1137_1138delinsGT (CLN5) NP_006484.1:p.Trp379=
NM_001366624.1:c.*439_*440delinsGT (CLN5) NP_001353553.1:n.*439_*440delinsGT
NM_006493.3:c.990_991delinsGT (CLN5) NP_006484.2:p.Trp330=
XM_017020538.2:c.644-7932_644-7931delinsAC (FBXL3) XP_016876027.1:n.644-7932_644-7931delinsAC
NM_001366624.2:c.*439_*440delinsGT (CLN5) NP_001353553.1:n.*439_*440delinsGT
NM_006493.4:c.990_991delinsGT (CLN5) MANE Select NP_006484.2:p.Trp330=