Canonical Allele Identifier: CA415086671

Gene: SLC6A8

Linked Data

• MyVariant Identifiers: chrX:g.152959589T>C (hg19) ; chrX:g.153694134T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153694134T>C , CM000685.2:g.153694134T>C	GRCh38
NC_000023.10:g.152959589T>C , CM000685.1:g.152959589T>C	GRCh37
NC_000023.9:g.152612783T>C	NCBI36
NG_012016.1:g.10838T>C
NG_012016.2:g.10838T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.1259T>C MANE Select	ENSP00000253122.5:p.Val420Ala
ENST00000253122.9:c.1259T>C	ENSP00000253122.5:p.Val420Ala
ENST00000413787.1:c.258-70T>C	ENSP00000400463.1:n.258-70T>C
ENST00000430077.6:c.914T>C	ENSP00000403041.2:p.Val305Ala
ENST00000442457.1:c.313T>C
ENST00000457723.1:c.239-3T>C	ENSP00000394742.1:n.239-3T>C
ENST00000485324.1:n.1404T>C
NM_001142805.1:c.1229T>C	NP_001136277.1:p.Val410Ala
NM_001142806.1:c.914T>C	NP_001136278.1:p.Val305Ala
NM_005629.3:c.1259T>C	NP_005620.1:p.Val420Ala
NM_005629.4:c.1259T>C MANE Select	NP_005620.1:p.Val420Ala
NM_001142805.2:c.1229T>C	NP_001136277.1:p.Val410Ala