Canonical Allele Identifier: CA415086462

Gene: SLC6A8

Linked Data

• gnomAD v4: X-153693970-G-A
• MyVariant Identifiers: chrX:g.152959425G>A (hg19) ; chrX:g.153693970G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153693970G>A , CM000685.2:g.153693970G>A	GRCh38
NC_000023.10:g.152959425G>A , CM000685.1:g.152959425G>A	GRCh37
NC_000023.9:g.152612619G>A	NCBI36
NG_012016.1:g.10674G>A
NG_012016.2:g.10674G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.1207G>A MANE Select	ENSP00000253122.5:p.Ala403Thr
ENST00000253122.9:c.1207G>A	ENSP00000253122.5:p.Ala403Thr
ENST00000413787.1:c.258-234G>A	ENSP00000400463.1:n.258-234G>A
ENST00000430077.6:c.862G>A	ENSP00000403041.2:p.Ala288Thr
ENST00000442457.1:c.261G>A
ENST00000457723.1:c.191G>A	ENSP00000394742.1:p.Gly64Asp
ENST00000467402.1:n.306G>A
ENST00000485324.1:n.1240G>A
NM_001142805.1:c.1177G>A	NP_001136277.1:p.Ala393Thr
NM_001142806.1:c.862G>A	NP_001136278.1:p.Ala288Thr
NM_005629.3:c.1207G>A	NP_005620.1:p.Ala403Thr
NM_005629.4:c.1207G>A MANE Select	NP_005620.1:p.Ala403Thr
NM_001142805.2:c.1177G>A	NP_001136277.1:p.Ala393Thr