Canonical Allele Identifier: CA519344858

Gene: SLC6A8

Linked Data

• MyVariant Identifiers: chrX:g.152959626C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153694171C>A , CM000685.2:g.153694171C>A	GRCh38
NC_000023.10:g.152959626C>A , CM000685.1:g.152959626C>A	GRCh37
NC_000023.9:g.152612820C>A	NCBI36
NG_012016.1:g.10875C>A
NG_012016.2:g.10875C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.1296C>A MANE Select	ENSP00000253122.5:p.Leu432=
ENST00000253122.9:c.1296C>A	ENSP00000253122.5:p.Leu432=
ENST00000413787.1:c.258-33C>A	ENSP00000400463.1:n.258-33C>A
ENST00000430077.6:c.951C>A	ENSP00000403041.2:p.Leu317=
ENST00000442457.1:c.350C>A
ENST00000485324.1:n.1441C>A
NM_001142805.1:c.1266C>A	NP_001136277.1:p.Leu422=
NM_001142806.1:c.951C>A	NP_001136278.1:p.Leu317=
NM_005629.3:c.1296C>A	NP_005620.1:p.Leu432=
NM_005629.4:c.1296C>A MANE Select	NP_005620.1:p.Leu432=
NM_001142805.2:c.1266C>A	NP_001136277.1:p.Leu422=