Canonical Allele Identifier: CA415075947

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153688606A>C , CM000685.2:g.153688606A>C GRCh38
NC_000023.10:g.152954061A>C , CM000685.1:g.152954061A>C GRCh37
NC_000023.9:g.152607255A>C NCBI36
NG_012016.1:g.5310A>C
NG_012016.2:g.5310A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000253122.10:c.32A>C (SLC6A8) MANE Select ENSP00000253122.5:p.Tyr11Ser
ENST00000253122.9:c.32A>C (SLC6A8) ENSP00000253122.5:p.Tyr11Ser
ENST00000458354.5:c.-3+209T>G (PNCK) ENSP00000401542.1:n.-3+209T>G
ENST00000480693.1:n.64+209T>G (PNCK)
NM_001142805.1:c.32A>C (SLC6A8) NP_001136277.1:p.Tyr11Ser
NM_005629.3:c.32A>C (SLC6A8) NP_005620.1:p.Tyr11Ser
NM_005629.4:c.32A>C (SLC6A8) MANE Select NP_005620.1:p.Tyr11Ser
NM_001142805.2:c.32A>C (SLC6A8) NP_001136277.1:p.Tyr11Ser