Canonical Allele Identifier: CA2695036134

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153688567_153688656del , CM000685.2:g.153688567_153688656del GRCh38
NC_000023.10:g.152954022_152954111del , CM000685.1:g.152954022_152954111del GRCh37
NC_000023.9:g.152607216_152607305del NCBI36
NG_012016.1:g.5271_5360del
NG_012016.2:g.5271_5360del

Transcript Alleles

HGVS Amino-acid Change
ENST00000253122.10:c.-8_82del (SLC6A8)
ENST00000253122.9:c.-8_82del (SLC6A8)
ENST00000458354.5:c.-3+165_-3+254del (PNCK) ENSP00000401542.1:n.-3+165_-3+254del
ENST00000480693.1:n.64+165_64+254del (PNCK)
NM_001142805.1:c.-8_82del (SLC6A8)
NM_005629.3:c.-8_82del (SLC6A8)
NM_005629.4:c.-8_82del (SLC6A8)
NM_001142805.2:c.-8_82del (SLC6A8)