Canonical Allele Identifier: CA415077486
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 3066438
ClinVar RCV Id: RCV003991442
gnomAD v4: X-153690413-G-A
MyVariant Identifiers: chrX:g.152955868G>A (hg19) chrX:g.153690413G>A (hg38)
ERepo: CA415077486/MONDO:0010305/027
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153690413G>A , CM000685.2:g.153690413G>A GRCh38
NC_000023.10:g.152955868G>A , CM000685.1:g.152955868G>A GRCh37
NC_000023.9:g.152609062G>A NCBI36
NG_012016.1:g.7117G>A
NG_012016.2:g.7117G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000253122.10:c.301G>A MANE Select ENSP00000253122.5:p.Gly101Arg
ENST00000675713.1:n.55G>A
ENST00000253122.9:c.301G>A ENSP00000253122.5:p.Gly101Arg
ENST00000430077.6:c.-45G>A ENSP00000403041.2:n.-45G>A
ENST00000476466.1:n.153G>A
NM_001142805.1:c.301G>A NP_001136277.1:p.Gly101Arg
NM_001142806.1:c.-45G>A NP_001136278.1:n.-45G>A
NM_005629.3:c.301G>A NP_005620.1:p.Gly101Arg
NM_005629.4:c.301G>A MANE Select NP_005620.1:p.Gly101Arg
NM_001142805.2:c.301G>A NP_001136277.1:p.Gly101Arg
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