Canonical Allele Identifier: CA2695036496

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153688746del , CM000685.2:g.153688746del GRCh38
NC_000023.10:g.152954201del , CM000685.1:g.152954201del GRCh37
NC_000023.9:g.152607395del NCBI36
NG_012016.1:g.5450del
NG_012016.2:g.5450del

Transcript Alleles

HGVS Amino-acid change
ENST00000253122.10:c.172del (SLC6A8) MANE Select ENSP00000253122.5:p.Gln58ArgfsTer?
ENST00000253122.9:c.172del (SLC6A8) ENSP00000253122.5:p.Gln58ArgfsTer?
ENST00000458354.5:c.-3+70del (PNCK) ENSP00000401542.1:n.-3+70del
ENST00000476466.1:n.24del (SLC6A8)
ENST00000480693.1:n.64+70del (PNCK)
NM_001142805.1:c.172del (SLC6A8) NP_001136277.1:p.Gln58ArgfsTer?
NM_005629.3:c.172del (SLC6A8) NP_005620.1:p.Gln58ArgfsTer?
NM_005629.4:c.172del (SLC6A8) MANE Select NP_005620.1:p.Gln58ArgfsTer?
NM_001142805.2:c.172del (SLC6A8) NP_001136277.1:p.Gln58ArgfsTer?