Canonical Allele Identifier: CA415086205

Gene: SLC6A8

Linked Data

• MyVariant Identifiers: chrX:g.152959384A>C (hg19) ; chrX:g.153693929A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153693929A>C , CM000685.2:g.153693929A>C	GRCh38
NC_000023.10:g.152959384A>C , CM000685.1:g.152959384A>C	GRCh37
NC_000023.9:g.152612578A>C	NCBI36
NG_012016.1:g.10633A>C
NG_012016.2:g.10633A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.1166A>C MANE Select	ENSP00000253122.5:p.Tyr389Ser
ENST00000253122.9:c.1166A>C	ENSP00000253122.5:p.Tyr389Ser
ENST00000413787.1:c.258-275A>C	ENSP00000400463.1:n.258-275A>C
ENST00000430077.6:c.821A>C	ENSP00000403041.2:p.Tyr274Ser
ENST00000442457.1:c.220A>C
ENST00000457723.1:c.150A>C	ENSP00000394742.1:p.Leu50=
ENST00000467402.1:n.265A>C
ENST00000485324.1:n.1199A>C
NM_001142805.1:c.1136A>C	NP_001136277.1:p.Tyr379Ser
NM_001142806.1:c.821A>C	NP_001136278.1:p.Tyr274Ser
NM_005629.3:c.1166A>C	NP_005620.1:p.Tyr389Ser
NM_005629.4:c.1166A>C MANE Select	NP_005620.1:p.Tyr389Ser
NM_001142805.2:c.1136A>C	NP_001136277.1:p.Tyr379Ser