Canonical Allele Identifier: CA2466438084
Gene: SLC6A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153693903A= , CM000685.2:g.153693903A= GRCh38
NC_000023.10:g.152959358A= , CM000685.1:g.152959358A= GRCh37
NC_000023.9:g.152612552A= NCBI36
NG_012016.1:g.10607A=
NG_012016.2:g.10607A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253122.10:c.1142-2A= MANE Select ENSP00000253122.5:n.1142-2A=
ENST00000253122.9:c.1142-2A= ENSP00000253122.5:n.1142-2A=
ENST00000413787.1:c.258-301A= ENSP00000400463.1:n.258-301A=
ENST00000430077.6:c.797-2A= ENSP00000403041.2:n.797-2A=
ENST00000442457.1:c.196-2A=
ENST00000457723.1:c.126-2A= ENSP00000394742.1:n.126-2A=
ENST00000467402.1:n.241-2A=
ENST00000485324.1:n.1175-2A=
NM_001142805.1:c.1112-2A= NP_001136277.1:n.1112-2A=
NM_001142806.1:c.797-2A= NP_001136278.1:n.797-2A=
NM_005629.3:c.1142-2A= NP_005620.1:n.1142-2A=
NM_005629.4:c.1142-2A= MANE Select NP_005620.1:n.1142-2A=
NM_001142805.2:c.1112-2A= NP_001136277.1:n.1112-2A=