Canonical Allele Identifier: CA415075981

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153688612T>G , CM000685.2:g.153688612T>G GRCh38
NC_000023.10:g.152954067T>G , CM000685.1:g.152954067T>G GRCh37
NC_000023.9:g.152607261T>G NCBI36
NG_012016.1:g.5316T>G
NG_012016.2:g.5316T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000253122.10:c.38T>G (SLC6A8) MANE Select ENSP00000253122.5:p.Val13Gly
ENST00000253122.9:c.38T>G (SLC6A8) ENSP00000253122.5:p.Val13Gly
ENST00000458354.5:c.-3+203A>C (PNCK) ENSP00000401542.1:n.-3+203A>C
ENST00000480693.1:n.64+203A>C (PNCK)
NM_001142805.1:c.38T>G (SLC6A8) NP_001136277.1:p.Val13Gly
NM_005629.3:c.38T>G (SLC6A8) NP_005620.1:p.Val13Gly
NM_005629.4:c.38T>G (SLC6A8) MANE Select NP_005620.1:p.Val13Gly
NM_001142805.2:c.38T>G (SLC6A8) NP_001136277.1:p.Val13Gly