Canonical Allele Identifier: CA415086278

Gene: SLC6A8

Linked Data

• MyVariant Identifiers: chrX:g.152959396T>A (hg19) ; chrX:g.153693941T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153693941T>A , CM000685.2:g.153693941T>A	GRCh38
NC_000023.10:g.152959396T>A , CM000685.1:g.152959396T>A	GRCh37
NC_000023.9:g.152612590T>A	NCBI36
NG_012016.1:g.10645T>A
NG_012016.2:g.10645T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.1178T>A MANE Select	ENSP00000253122.5:p.Val393Asp
ENST00000253122.9:c.1178T>A	ENSP00000253122.5:p.Val393Asp
ENST00000413787.1:c.258-263T>A	ENSP00000400463.1:n.258-263T>A
ENST00000430077.6:c.833T>A	ENSP00000403041.2:p.Val278Asp
ENST00000442457.1:c.232T>A
ENST00000457723.1:c.162T>A	ENSP00000394742.1:p.Cys54Ter
ENST00000467402.1:n.277T>A
ENST00000485324.1:n.1211T>A
NM_001142805.1:c.1148T>A	NP_001136277.1:p.Val383Asp
NM_001142806.1:c.833T>A	NP_001136278.1:p.Val278Asp
NM_005629.3:c.1178T>A	NP_005620.1:p.Val393Asp
NM_005629.4:c.1178T>A MANE Select	NP_005620.1:p.Val393Asp
NM_001142805.2:c.1148T>A	NP_001136277.1:p.Val383Asp