Canonical Allele Identifier: CA415087934
Community Standard Title: NM_005629.4(SLC6A8):c.1494C>G (p.Tyr498Ter)
Gene: SLC6A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153694445C>G , CM000685.2:g.153694445C>G GRCh38
NC_000023.10:g.152959900C>G , CM000685.1:g.152959900C>G GRCh37
NC_000023.9:g.152613094C>G NCBI36
NG_012016.1:g.11149C>G
NG_012016.2:g.11149C>G

Transcript Alleles

HGVS Amino-acid Change
NM_005629.4:c.1494C>G MANE Select NP_005620.1:p.Tyr498Ter
ENST00000253122.10:c.1494C>G MANE Select ENSP00000253122.5:p.Tyr498Ter
NM_001142805.1:c.1464C>G NP_001136277.1:p.Tyr488Ter
NM_001142805.2:c.1464C>G NP_001136277.1:p.Tyr488Ter
NM_001142806.1:c.1149C>G NP_001136278.1:p.Tyr383Ter
NM_005629.3:c.1494C>G NP_005620.1:p.Tyr498Ter
ENST00000253122.9:c.1494C>G ENSP00000253122.5:p.Tyr498Ter
ENST00000413787.1:c.423C>G ENSP00000400463.1:p.Tyr141Ter
ENST00000430077.6:c.1149C>G ENSP00000403041.2:p.Tyr383Ter
ENST00000485324.1:n.1715C>G