Canonical Allele Identifier: CA519184979

Gene: SLC6A8

Linked Data

• gnomAD v4: X-153690469-C-T
• MyVariant Identifiers: chrX:g.152955924C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153690469C>T , CM000685.2:g.153690469C>T	GRCh38
NC_000023.10:g.152955924C>T , CM000685.1:g.152955924C>T	GRCh37
NC_000023.9:g.152609118C>T	NCBI36
NG_012016.1:g.7173C>T
NG_012016.2:g.7173C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.357C>T MANE Select	ENSP00000253122.5:p.Gly119=
ENST00000675713.1:n.111C>T
ENST00000253122.9:c.357C>T	ENSP00000253122.5:p.Gly119=
ENST00000430077.6:c.12C>T	ENSP00000403041.2:p.Gly4=
ENST00000476466.1:n.209C>T
NM_001142805.1:c.357C>T	NP_001136277.1:p.Gly119=
NM_001142806.1:c.12C>T	NP_001136278.1:p.Gly4=
NM_005629.3:c.357C>T	NP_005620.1:p.Gly119=
NM_005629.4:c.357C>T MANE Select	NP_005620.1:p.Gly119=
NM_001142805.2:c.357C>T	NP_001136277.1:p.Gly119=