Canonical Allele Identifier: CA2740040899
Gene: SLC6A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153694305G>T , CM000685.2:g.153694305G>T GRCh38
NC_000023.10:g.152959760G>T , CM000685.1:g.152959760G>T GRCh37
NC_000023.9:g.152612954G>T NCBI36
NG_012016.1:g.11009G>T
NG_012016.2:g.11009G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000253122.10:c.1393-39G>T MANE Select ENSP00000253122.5:n.1393-39G>T
ENST00000253122.9:c.1393-39G>T ENSP00000253122.5:n.1393-39G>T
ENST00000413787.1:c.322-39G>T ENSP00000400463.1:n.322-39G>T
ENST00000430077.6:c.1048-39G>T ENSP00000403041.2:n.1048-39G>T
ENST00000442457.1:c.447-39G>T
ENST00000485324.1:n.1575G>T
NM_001142805.1:c.1363-39G>T NP_001136277.1:n.1363-39G>T
NM_001142806.1:c.1048-39G>T NP_001136278.1:n.1048-39G>T
NM_005629.3:c.1393-39G>T NP_005620.1:n.1393-39G>T
NM_005629.4:c.1393-39G>T MANE Select NP_005620.1:n.1393-39G>T
NM_001142805.2:c.1363-39G>T NP_001136277.1:n.1363-39G>T