Canonical Allele Identifier: CA415077505

Gene: SLC6A8

Linked Data

• gnomAD v4: X-153690416-G-T
• MyVariant Identifiers: chrX:g.152955871G>T (hg19) ; chrX:g.153690416G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153690416G>T , CM000685.2:g.153690416G>T	GRCh38
NC_000023.10:g.152955871G>T , CM000685.1:g.152955871G>T	GRCh37
NC_000023.9:g.152609065G>T	NCBI36
NG_012016.1:g.7120G>T
NG_012016.2:g.7120G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.304G>T MANE Select	ENSP00000253122.5:p.Gly102Ter
ENST00000675713.1:n.58G>T
ENST00000253122.9:c.304G>T	ENSP00000253122.5:p.Gly102Ter
ENST00000430077.6:c.-42G>T	ENSP00000403041.2:n.-42G>T
ENST00000476466.1:n.156G>T
NM_001142805.1:c.304G>T	NP_001136277.1:p.Gly102Ter
NM_001142806.1:c.-42G>T	NP_001136278.1:n.-42G>T
NM_005629.3:c.304G>T	NP_005620.1:p.Gly102Ter
NM_005629.4:c.304G>T MANE Select	NP_005620.1:p.Gly102Ter
NM_001142805.2:c.304G>T	NP_001136277.1:p.Gly102Ter