Canonical Allele Identifier: CA415075922

Linked Data

ClinVar Variation Id: 571505
dbSNP Id: rs1198790754

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153688600G>T , CM000685.2:g.153688600G>T GRCh38
NC_000023.10:g.152954055G>T , CM000685.1:g.152954055G>T GRCh37
NC_000023.9:g.152607249G>T NCBI36
NG_012016.1:g.5304G>T
NG_012016.2:g.5304G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000253122.10:c.26G>T (SLC6A8) MANE Select ENSP00000253122.5:p.Gly9Val
ENST00000253122.9:c.26G>T (SLC6A8) ENSP00000253122.5:p.Gly9Val
ENST00000458354.5:c.-3+215C>A (PNCK) ENSP00000401542.1:n.-3+215C>A
ENST00000480693.1:n.64+215C>A (PNCK)
NM_001142805.1:c.26G>T (SLC6A8) NP_001136277.1:p.Gly9Val
NM_005629.3:c.26G>T (SLC6A8) NP_005620.1:p.Gly9Val
NM_005629.4:c.26G>T (SLC6A8) MANE Select NP_005620.1:p.Gly9Val
NM_001142805.2:c.26G>T (SLC6A8) NP_001136277.1:p.Gly9Val