Canonical Allele Identifier: CA415087005

Gene: SLC6A8

Linked Data

• MyVariant Identifiers: chrX:g.152959694T>A (hg19) ; chrX:g.153694239T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153694239T>A , CM000685.2:g.153694239T>A	GRCh38
NC_000023.10:g.152959694T>A , CM000685.1:g.152959694T>A	GRCh37
NC_000023.9:g.152612888T>A	NCBI36
NG_012016.1:g.10943T>A
NG_012016.2:g.10943T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.1364T>A MANE Select	ENSP00000253122.5:p.Phe455Tyr
ENST00000253122.9:c.1364T>A	ENSP00000253122.5:p.Phe455Tyr
ENST00000413787.1:c.293T>A	ENSP00000400463.1:p.Phe98Tyr
ENST00000430077.6:c.1019T>A	ENSP00000403041.2:p.Phe340Tyr
ENST00000442457.1:c.418T>A
ENST00000485324.1:n.1509T>A
NM_001142805.1:c.1334T>A	NP_001136277.1:p.Phe445Tyr
NM_001142806.1:c.1019T>A	NP_001136278.1:p.Phe340Tyr
NM_005629.3:c.1364T>A	NP_005620.1:p.Phe455Tyr
NM_005629.4:c.1364T>A MANE Select	NP_005620.1:p.Phe455Tyr
NM_001142805.2:c.1334T>A	NP_001136277.1:p.Phe445Tyr