Canonical Allele Identifier: CA2466436601
Gene: SLC6A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153690437G= , CM000685.2:g.153690437G= GRCh38
NC_000023.10:g.152955892G= , CM000685.1:g.152955892G= GRCh37
NC_000023.9:g.152609086G= NCBI36
NG_012016.1:g.7141G=
NG_012016.2:g.7141G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253122.10:c.325G= MANE Select ENSP00000253122.5:p.Glu109=
ENST00000675713.1:n.79G=
ENST00000253122.9:c.325G= ENSP00000253122.5:p.Glu109=
ENST00000430077.6:c.-21G= ENSP00000403041.2:n.-21G=
ENST00000476466.1:n.177G=
NM_001142805.1:c.325G= NP_001136277.1:p.Glu109=
NM_001142806.1:c.-21G= NP_001136278.1:n.-21G=
NM_005629.3:c.325G= NP_005620.1:p.Glu109=
NM_005629.4:c.325G= MANE Select NP_005620.1:p.Glu109=
NM_001142805.2:c.325G= NP_001136277.1:p.Glu109=