Canonical Allele Identifier: CA2466438189
Gene: SLC6A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153694115C= , CM000685.2:g.153694115C= GRCh38
NC_000023.10:g.152959570C= , CM000685.1:g.152959570C= GRCh37
NC_000023.9:g.152612764C= NCBI36
NG_012016.1:g.10819C=
NG_012016.2:g.10819C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253122.10:c.1255-15C= MANE Select ENSP00000253122.5:n.1255-15C=
ENST00000253122.9:c.1255-15C= ENSP00000253122.5:n.1255-15C=
ENST00000413787.1:c.258-89C= ENSP00000400463.1:n.258-89C=
ENST00000430077.6:c.910-15C= ENSP00000403041.2:n.910-15C=
ENST00000442457.1:c.309-15C=
ENST00000457723.1:c.239-22C= ENSP00000394742.1:n.239-22C=
ENST00000485324.1:n.1385C=
NM_001142805.1:c.1225-15C= NP_001136277.1:n.1225-15C=
NM_001142806.1:c.910-15C= NP_001136278.1:n.910-15C=
NM_005629.3:c.1255-15C= NP_005620.1:n.1255-15C=
NM_005629.4:c.1255-15C= MANE Select NP_005620.1:n.1255-15C=
NM_001142805.2:c.1225-15C= NP_001136277.1:n.1225-15C=