Canonical Allele Identifier: CA658659052
Community Standard Title: NM_005629.4(SLC6A8):c.1393-8T>G
Gene: SLC6A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153694336T>G , CM000685.2:g.153694336T>G GRCh38
NC_000023.10:g.152959791T>G , CM000685.1:g.152959791T>G GRCh37
NC_000023.9:g.152612985T>G NCBI36
NG_012016.1:g.11040T>G
NG_012016.2:g.11040T>G

Transcript Alleles

HGVS Amino-acid Change
NM_005629.4:c.1393-8T>G MANE Select NP_005620.1:n.1393-8T>G
ENST00000253122.10:c.1393-8T>G MANE Select ENSP00000253122.5:n.1393-8T>G
NM_001142805.1:c.1363-8T>G NP_001136277.1:n.1363-8T>G
NM_001142805.2:c.1363-8T>G NP_001136277.1:n.1363-8T>G
NM_001142806.1:c.1048-8T>G NP_001136278.1:n.1048-8T>G
NM_005629.3:c.1393-8T>G NP_005620.1:n.1393-8T>G
ENST00000253122.9:c.1393-8T>G ENSP00000253122.5:n.1393-8T>G
ENST00000413787.1:c.322-8T>G ENSP00000400463.1:n.322-8T>G
ENST00000430077.6:c.1048-8T>G ENSP00000403041.2:n.1048-8T>G
ENST00000442457.1:c.447-8T>G
ENST00000485324.1:n.1606T>G