Canonical Allele Identifier: CA415086548

Gene: SLC6A8

Linked Data

• MyVariant Identifiers: chrX:g.152959438T>G (hg19) ; chrX:g.153693983T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153693983T>G , CM000685.2:g.153693983T>G	GRCh38
NC_000023.10:g.152959438T>G , CM000685.1:g.152959438T>G	GRCh37
NC_000023.9:g.152612632T>G	NCBI36
NG_012016.1:g.10687T>G
NG_012016.2:g.10687T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.1220T>G MANE Select	ENSP00000253122.5:p.Phe407Cys
ENST00000253122.9:c.1220T>G	ENSP00000253122.5:p.Phe407Cys
ENST00000413787.1:c.258-221T>G	ENSP00000400463.1:n.258-221T>G
ENST00000430077.6:c.875T>G	ENSP00000403041.2:p.Phe292Cys
ENST00000442457.1:c.274T>G
ENST00000457723.1:c.204T>G	ENSP00000394742.1:p.Leu68=
ENST00000485324.1:n.1253T>G
NM_001142805.1:c.1190T>G	NP_001136277.1:p.Phe397Cys
NM_001142806.1:c.875T>G	NP_001136278.1:p.Phe292Cys
NM_005629.3:c.1220T>G	NP_005620.1:p.Phe407Cys
NM_005629.4:c.1220T>G MANE Select	NP_005620.1:p.Phe407Cys
NM_001142805.2:c.1190T>G	NP_001136277.1:p.Phe397Cys