Canonical Allele Identifier: CA415086717

Gene: SLC6A8

Linked Data

• MyVariant Identifiers: chrX:g.152959609A>G (hg19) ; chrX:g.153694154A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153694154A>G , CM000685.2:g.153694154A>G	GRCh38
NC_000023.10:g.152959609A>G , CM000685.1:g.152959609A>G	GRCh37
NC_000023.9:g.152612803A>G	NCBI36
NG_012016.1:g.10858A>G
NG_012016.2:g.10858A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.1279A>G MANE Select	ENSP00000253122.5:p.Thr427Ala
ENST00000253122.9:c.1279A>G	ENSP00000253122.5:p.Thr427Ala
ENST00000413787.1:c.258-50A>G	ENSP00000400463.1:n.258-50A>G
ENST00000430077.6:c.934A>G	ENSP00000403041.2:p.Thr312Ala
ENST00000442457.1:c.333A>G
ENST00000457723.1:c.256A>G	ENSP00000394742.1:p.Thr86Ala
ENST00000485324.1:n.1424A>G
NM_001142805.1:c.1249A>G	NP_001136277.1:p.Thr417Ala
NM_001142806.1:c.934A>G	NP_001136278.1:p.Thr312Ala
NM_005629.3:c.1279A>G	NP_005620.1:p.Thr427Ala
NM_005629.4:c.1279A>G MANE Select	NP_005620.1:p.Thr427Ala
NM_001142805.2:c.1249A>G	NP_001136277.1:p.Thr417Ala