Canonical Allele Identifier: CA415086265

Gene: SLC6A8

Linked Data

• MyVariant Identifiers: chrX:g.152959394T>G (hg19) ; chrX:g.153693939T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153693939T>G , CM000685.2:g.153693939T>G	GRCh38
NC_000023.10:g.152959394T>G , CM000685.1:g.152959394T>G	GRCh37
NC_000023.9:g.152612588T>G	NCBI36
NG_012016.1:g.10643T>G
NG_012016.2:g.10643T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.1176T>G MANE Select	ENSP00000253122.5:p.Ala392=
ENST00000253122.9:c.1176T>G	ENSP00000253122.5:p.Ala392=
ENST00000413787.1:c.258-265T>G	ENSP00000400463.1:n.258-265T>G
ENST00000430077.6:c.831T>G	ENSP00000403041.2:p.Ala277=
ENST00000442457.1:c.230T>G
ENST00000457723.1:c.160T>G	ENSP00000394742.1:p.Cys54Gly
ENST00000467402.1:n.275T>G
ENST00000485324.1:n.1209T>G
NM_001142805.1:c.1146T>G	NP_001136277.1:p.Ala382=
NM_001142806.1:c.831T>G	NP_001136278.1:p.Ala277=
NM_005629.3:c.1176T>G	NP_005620.1:p.Ala392=
NM_005629.4:c.1176T>G MANE Select	NP_005620.1:p.Ala392=
NM_001142805.2:c.1146T>G	NP_001136277.1:p.Ala382=