Canonical Allele Identifier: CA519344945

Gene: SLC6A8

Linked Data

• COSMIC: COSM6186149
• MyVariant Identifiers: chrX:g.152959710C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153694255C>G , CM000685.2:g.153694255C>G	GRCh38
NC_000023.10:g.152959710C>G , CM000685.1:g.152959710C>G	GRCh37
NC_000023.9:g.152612904C>G	NCBI36
NG_012016.1:g.10959C>G
NG_012016.2:g.10959C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.1380C>G MANE Select	ENSP00000253122.5:p.Ser460=
ENST00000253122.9:c.1380C>G	ENSP00000253122.5:p.Ser460=
ENST00000413787.1:c.309C>G	ENSP00000400463.1:p.Ser103=
ENST00000430077.6:c.1035C>G	ENSP00000403041.2:p.Ser345=
ENST00000442457.1:c.434C>G
ENST00000485324.1:n.1525C>G
NM_001142805.1:c.1350C>G	NP_001136277.1:p.Ser450=
NM_001142806.1:c.1035C>G	NP_001136278.1:p.Ser345=
NM_005629.3:c.1380C>G	NP_005620.1:p.Ser460=
NM_005629.4:c.1380C>G MANE Select	NP_005620.1:p.Ser460=
NM_001142805.2:c.1350C>G	NP_001136277.1:p.Ser450=