Canonical Allele Identifier: CA415086098

Gene: SLC6A8

Linked Data

• MyVariant Identifiers: chrX:g.152959367C>G (hg19) ; chrX:g.153693912C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153693912C>G , CM000685.2:g.153693912C>G	GRCh38
NC_000023.10:g.152959367C>G , CM000685.1:g.152959367C>G	GRCh37
NC_000023.9:g.152612561C>G	NCBI36
NG_012016.1:g.10616C>G
NG_012016.2:g.10616C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.1149C>G MANE Select	ENSP00000253122.5:p.Gly383=
ENST00000253122.9:c.1149C>G	ENSP00000253122.5:p.Gly383=
ENST00000413787.1:c.258-292C>G	ENSP00000400463.1:n.258-292C>G
ENST00000430077.6:c.804C>G	ENSP00000403041.2:p.Gly268=
ENST00000442457.1:c.203C>G
ENST00000457723.1:c.133C>G	ENSP00000394742.1:p.Pro45Ala
ENST00000467402.1:n.248C>G
ENST00000485324.1:n.1182C>G
NM_001142805.1:c.1119C>G	NP_001136277.1:p.Gly373=
NM_001142806.1:c.804C>G	NP_001136278.1:p.Gly268=
NM_005629.3:c.1149C>G	NP_005620.1:p.Gly383=
NM_005629.4:c.1149C>G MANE Select	NP_005620.1:p.Gly383=
NM_001142805.2:c.1119C>G	NP_001136277.1:p.Gly373=