Canonical Allele Identifier: CA2466438109

Gene: SLC6A8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153693970G= , CM000685.2:g.153693970G=	GRCh38
NC_000023.10:g.152959425G= , CM000685.1:g.152959425G=	GRCh37
NC_000023.9:g.152612619G=	NCBI36
NG_012016.1:g.10674G=
NG_012016.2:g.10674G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.1207G= MANE Select	ENSP00000253122.5:p.Ala403=
ENST00000253122.9:c.1207G=	ENSP00000253122.5:p.Ala403=
ENST00000413787.1:c.258-234G=	ENSP00000400463.1:n.258-234G=
ENST00000430077.6:c.862G=	ENSP00000403041.2:p.Ala288=
ENST00000442457.1:c.261G=
ENST00000457723.1:c.191G=	ENSP00000394742.1:p.Gly64=
ENST00000467402.1:n.306G=
ENST00000485324.1:n.1240G=
NM_001142805.1:c.1177G=	NP_001136277.1:p.Ala393=
NM_001142806.1:c.862G=	NP_001136278.1:p.Ala288=
NM_005629.3:c.1207G=	NP_005620.1:p.Ala403=
NM_005629.4:c.1207G= MANE Select	NP_005620.1:p.Ala403=
NM_001142805.2:c.1177G=	NP_001136277.1:p.Ala393=