Canonical Allele Identifier: CA519344388
Gene: SLC6A8 HGNC NCBI
PNCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1536022
ClinVar RCV Id: RCV002090185
dbSNP Id: rs1057524586
gnomAD v2: X-152954077-C-T
gnomAD v3: X-153688622-C-T
gnomAD v4: X-153688622-C-T
MyVariant Identifiers: chrX:g.152954077C>T (hg19) chrX:g.153688622C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153688622C>T , CM000685.2:g.153688622C>T GRCh38
NC_000023.10:g.152954077C>T , CM000685.1:g.152954077C>T GRCh37
NC_000023.9:g.152607271C>T NCBI36
NG_012016.1:g.5326C>T
NG_012016.2:g.5326C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000253122.10:c.48C>T (SLC6A8) MANE Select ENSP00000253122.5:p.Asp16=
ENST00000253122.9:c.48C>T (SLC6A8) ENSP00000253122.5:p.Asp16=
ENST00000458354.5:c.-3+193G>A (PNCK) ENSP00000401542.1:n.-3+193G>A
ENST00000480693.1:n.64+193G>A (PNCK)
NM_001142805.1:c.48C>T (SLC6A8) NP_001136277.1:p.Asp16=
NM_005629.3:c.48C>T (SLC6A8) NP_005620.1:p.Asp16=
NM_005629.4:c.48C>T (SLC6A8) MANE Select NP_005620.1:p.Asp16=
NM_001142805.2:c.48C>T (SLC6A8) NP_001136277.1:p.Asp16=
Search 100 bp 5'
Search 100 bp 3'