Canonical Allele Identifier: CA415085342

Gene: SLC6A8

Linked Data

• MyVariant Identifiers: chrX:g.152958952C>G (hg19) ; chrX:g.153693497C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153693497C>G , CM000685.2:g.153693497C>G	GRCh38
NC_000023.10:g.152958952C>G , CM000685.1:g.152958952C>G	GRCh37
NC_000023.9:g.152612146C>G	NCBI36
NG_012016.1:g.10201C>G
NG_012016.2:g.10201C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000253122.10:c.1052C>G MANE Select	ENSP00000253122.5:p.Thr351Ser
ENST00000253122.9:c.1052C>G	ENSP00000253122.5:p.Thr351Ser
ENST00000413787.1:c.168C>G	ENSP00000400463.1:p.Asp56Glu
ENST00000430077.6:c.707C>G	ENSP00000403041.2:p.Thr236Ser
ENST00000442457.1:c.106C>G
ENST00000457723.1:c.36C>G	ENSP00000394742.1:p.Asp12Glu
ENST00000467402.1:n.151C>G
ENST00000485324.1:n.1085C>G
NM_001142805.1:c.1022C>G	NP_001136277.1:p.Thr341Ser
NM_001142806.1:c.707C>G	NP_001136278.1:p.Thr236Ser
NM_005629.3:c.1052C>G	NP_005620.1:p.Thr351Ser
NM_005629.4:c.1052C>G MANE Select	NP_005620.1:p.Thr351Ser
NM_001142805.2:c.1022C>G	NP_001136277.1:p.Thr341Ser