Canonical Allele Identifier: CA2499226441
Community Standard Title: NM_005629.4(SLC6A8):c.1551del (p.Trp518GlyfsTer2)
Gene: SLC6A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153694588del , CM000685.2:g.153694588del GRCh38
NC_000023.10:g.152960043del , CM000685.1:g.152960043del GRCh37
NC_000023.9:g.152613237del NCBI36
NG_012016.1:g.11292del
NG_012016.2:g.11292del

Transcript Alleles

HGVS Amino-acid Change
NM_005629.4:c.1551del MANE Select NP_005620.1:p.Trp518GlyfsTer2
ENST00000253122.10:c.1551del MANE Select ENSP00000253122.5:p.Trp518GlyfsTer2
NM_001142805.1:c.1521del NP_001136277.1:p.Trp508GlyfsTer2
NM_001142805.2:c.1521del NP_001136277.1:p.Trp508GlyfsTer2
NM_001142806.1:c.1206del NP_001136278.1:p.Trp403GlyfsTer2
NM_005629.3:c.1551del NP_005620.1:p.Trp518GlyfsTer2
ENST00000253122.9:c.1551del ENSP00000253122.5:p.Trp518GlyfsTer2
ENST00000430077.6:c.1206del ENSP00000403041.2:p.Trp403GlyfsTer2
ENST00000485324.1:n.1858del