Canonical Allele Identifier: CA2466438092

Gene: SLC6A8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153693925G= , CM000685.2:g.153693925G=	GRCh38
NC_000023.10:g.152959380G= , CM000685.1:g.152959380G=	GRCh37
NC_000023.9:g.152612574G=	NCBI36
NG_012016.1:g.10629G=
NG_012016.2:g.10629G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.1162G= MANE Select	ENSP00000253122.5:p.Ala388=
ENST00000253122.9:c.1162G=	ENSP00000253122.5:p.Ala388=
ENST00000413787.1:c.258-279G=	ENSP00000400463.1:n.258-279G=
ENST00000430077.6:c.817G=	ENSP00000403041.2:p.Ala273=
ENST00000442457.1:c.216G=
ENST00000457723.1:c.146G=	ENSP00000394742.1:p.Arg49=
ENST00000467402.1:n.261G=
ENST00000485324.1:n.1195G=
NM_001142805.1:c.1132G=	NP_001136277.1:p.Ala378=
NM_001142806.1:c.817G=	NP_001136278.1:p.Ala273=
NM_005629.3:c.1162G=	NP_005620.1:p.Ala388=
NM_005629.4:c.1162G= MANE Select	NP_005620.1:p.Ala388=
NM_001142805.2:c.1132G=	NP_001136277.1:p.Ala378=