Canonical Allele Identifier: CA415086770

Gene: SLC6A8

Linked Data

• dbSNP Id: rs1557045395
• gnomAD v2: X-152959634-C-T
• gnomAD v4: X-153694179-C-T
• MyVariant Identifiers: chrX:g.152959634C>T (hg19) ; chrX:g.153694179C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153694179C>T , CM000685.2:g.153694179C>T	GRCh38
NC_000023.10:g.152959634C>T , CM000685.1:g.152959634C>T	GRCh37
NC_000023.9:g.152612828C>T	NCBI36
NG_012016.1:g.10883C>T
NG_012016.2:g.10883C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.1304C>T MANE Select	ENSP00000253122.5:p.Ala435Val
ENST00000253122.9:c.1304C>T	ENSP00000253122.5:p.Ala435Val
ENST00000413787.1:c.258-25C>T	ENSP00000400463.1:n.258-25C>T
ENST00000430077.6:c.959C>T	ENSP00000403041.2:p.Ala320Val
ENST00000442457.1:c.358C>T
ENST00000485324.1:n.1449C>T
NM_001142805.1:c.1274C>T	NP_001136277.1:p.Ala425Val
NM_001142806.1:c.959C>T	NP_001136278.1:p.Ala320Val
NM_005629.3:c.1304C>T	NP_005620.1:p.Ala435Val
NM_005629.4:c.1304C>T MANE Select	NP_005620.1:p.Ala435Val
NM_001142805.2:c.1274C>T	NP_001136277.1:p.Ala425Val