Canonical Allele Identifier: CA415086397

Gene: SLC6A8

Linked Data

• gnomAD v4: X-153693959-C-A
• MyVariant Identifiers: chrX:g.152959414C>A (hg19) ; chrX:g.153693959C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153693959C>A , CM000685.2:g.153693959C>A	GRCh38
NC_000023.10:g.152959414C>A , CM000685.1:g.152959414C>A	GRCh37
NC_000023.9:g.152612608C>A	NCBI36
NG_012016.1:g.10663C>A
NG_012016.2:g.10663C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.1196C>A MANE Select	ENSP00000253122.5:p.Ala399Asp
ENST00000253122.9:c.1196C>A	ENSP00000253122.5:p.Ala399Asp
ENST00000413787.1:c.258-245C>A	ENSP00000400463.1:n.258-245C>A
ENST00000430077.6:c.851C>A	ENSP00000403041.2:p.Ala284Asp
ENST00000442457.1:c.250C>A
ENST00000457723.1:c.180C>A	ENSP00000394742.1:p.Gly60=
ENST00000467402.1:n.295C>A
ENST00000485324.1:n.1229C>A
NM_001142805.1:c.1166C>A	NP_001136277.1:p.Ala389Asp
NM_001142806.1:c.851C>A	NP_001136278.1:p.Ala284Asp
NM_005629.3:c.1196C>A	NP_005620.1:p.Ala399Asp
NM_005629.4:c.1196C>A MANE Select	NP_005620.1:p.Ala399Asp
NM_001142805.2:c.1166C>A	NP_001136277.1:p.Ala389Asp