Canonical Allele Identifier: CA415077382

Gene: SLC6A8

Linked Data

• MyVariant Identifiers: chrX:g.152955850G>T (hg19) ; chrX:g.153690395G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153690395G>T , CM000685.2:g.153690395G>T	GRCh38
NC_000023.10:g.152955850G>T , CM000685.1:g.152955850G>T	GRCh37
NC_000023.9:g.152609044G>T	NCBI36
NG_012016.1:g.7099G>T
NG_012016.2:g.7099G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.283G>T MANE Select	ENSP00000253122.5:p.Val95Phe
ENST00000675713.1:n.37G>T
ENST00000253122.9:c.283G>T	ENSP00000253122.5:p.Val95Phe
ENST00000430077.6:c.-63G>T	ENSP00000403041.2:n.-63G>T
ENST00000476466.1:n.135G>T
NM_001142805.1:c.283G>T	NP_001136277.1:p.Val95Phe
NM_001142806.1:c.-63G>T	NP_001136278.1:n.-63G>T
NM_005629.3:c.283G>T	NP_005620.1:p.Val95Phe
NM_005629.4:c.283G>T MANE Select	NP_005620.1:p.Val95Phe
NM_001142805.2:c.283G>T	NP_001136277.1:p.Val95Phe