Canonical Allele Identifier: CA484486542

Linked Data

MyVariant Identifiers: chr13:g.77570150T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.76996015T>A , CM000675.2:g.76996015T>A GRCh38
NC_000013.10:g.77570150T>A , CM000675.1:g.77570150T>A GRCh37
NC_000013.9:g.76468151T>A NCBI36
NG_009064.1:g.9092T>A , LRG_692:g.9092T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000377453.9:c.453T>A (CLN5) MANE Select ENSP00000366673.5:p.Pro151=
ENST00000485938.4:c.453T>A (CLN5) ENSP00000482959.3:p.Pro151=
ENST00000616833.6:c.453T>A (CLN5) ENSP00000479547.3:p.Pro151=
ENST00000635838.1:c.62T>A
ENST00000635905.1:n.454T>A (CLN5)
ENST00000635915.1:c.451T>A (CLN5)
ENST00000635989.1:n.520T>A (CLN5)
ENST00000636183.2:c.453T>A (CLN5) ENSP00000490181.2:p.Pro151=
ENST00000636520.1:n.1965T>A (CLN5)
ENST00000636525.2:c.453T>A (CLN5) ENSP00000490078.2:p.Pro151=
ENST00000636602.1:n.399T>A (CLN5)
ENST00000636681.1:c.*144T>A (CLN5) ENSP00000489922.1:n.*144T>A
ENST00000636705.1:c.289T>A (CLN5)
ENST00000636767.2:c.453T>A (CLN5) ENSP00000489855.2:p.Pro151=
ENST00000636780.2:c.453T>A (CLN5) ENSP00000489809.2:p.Pro151=
ENST00000637192.1:c.101T>A
ENST00000637278.1:n.779T>A (CLN5)
ENST00000637397.2:c.453T>A (CLN5) ENSP00000490422.2:p.Pro151=
ENST00000637537.2:c.453T>A (CLN5) ENSP00000489711.2:p.Pro151=
ENST00000638101.1:c.57T>A ENSP00000490535.1:p.Pro19=
ENST00000638147.2:c.453T>A ENSP00000490953.2:p.Pro151=
ENST00000377453.7:c.600T>A (CLN5) ENSP00000366673.3:p.Pro200=
ENST00000485797.2:n.174-3064A>T (FBXL3)
ENST00000485938.2:c.436T>A (CLN5)
ENST00000616833.4:c.453T>A (CLN5) ENSP00000479547.1:p.Pro151=
NM_006493.2:c.600T>A , LRG_692t1:c.600T>A (CLN5) NP_006484.1:p.Pro200=
XM_011534917.1:c.600T>A (CLN5) XP_011533219.1:p.Pro200=
NM_001366624.1:c.453T>A (CLN5) NP_001353553.1:p.Pro151=
NM_006493.3:c.453T>A (CLN5) NP_006484.2:p.Pro151=
XM_017020538.2:c.644-3064A>T (FBXL3) XP_016876027.1:n.644-3064A>T
NM_001366624.2:c.453T>A (CLN5) NP_001353553.1:p.Pro151=
NM_006493.4:c.453T>A (CLN5) MANE Select NP_006484.2:p.Pro151=