Canonical Allele Identifier: CA415086627

Gene: SLC6A8

Linked Data

• MyVariant Identifiers: chrX:g.152959465A>T (hg19) ; chrX:g.153694010A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153694010A>T , CM000685.2:g.153694010A>T	GRCh38
NC_000023.10:g.152959465A>T , CM000685.1:g.152959465A>T	GRCh37
NC_000023.9:g.152612659A>T	NCBI36
NG_012016.1:g.10714A>T
NG_012016.2:g.10714A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.1247A>T MANE Select	ENSP00000253122.5:p.Asp416Val
ENST00000253122.9:c.1247A>T	ENSP00000253122.5:p.Asp416Val
ENST00000413787.1:c.258-194A>T	ENSP00000400463.1:n.258-194A>T
ENST00000430077.6:c.902A>T	ENSP00000403041.2:p.Asp301Val
ENST00000442457.1:c.301A>T
ENST00000457723.1:c.231A>T	ENSP00000394742.1:p.Arg77=
ENST00000485324.1:n.1280A>T
NM_001142805.1:c.1217A>T	NP_001136277.1:p.Asp406Val
NM_001142806.1:c.902A>T	NP_001136278.1:p.Asp301Val
NM_005629.3:c.1247A>T	NP_005620.1:p.Asp416Val
NM_005629.4:c.1247A>T MANE Select	NP_005620.1:p.Asp416Val
NM_001142805.2:c.1217A>T	NP_001136277.1:p.Asp406Val