Canonical Allele Identifier: CA415077761

Gene: SLC6A8

Linked Data

• gnomAD v4: X-153690456-T-C
• MyVariant Identifiers: chrX:g.152955911T>C (hg19) ; chrX:g.153690456T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153690456T>C , CM000685.2:g.153690456T>C	GRCh38
NC_000023.10:g.152955911T>C , CM000685.1:g.152955911T>C	GRCh37
NC_000023.9:g.152609105T>C	NCBI36
NG_012016.1:g.7160T>C
NG_012016.2:g.7160T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.344T>C MANE Select	ENSP00000253122.5:p.Phe115Ser
ENST00000675713.1:n.98T>C
ENST00000253122.9:c.344T>C	ENSP00000253122.5:p.Phe115Ser
ENST00000430077.6:c.-2T>C	ENSP00000403041.2:n.-2T>C
ENST00000476466.1:n.196T>C
NM_001142805.1:c.344T>C	NP_001136277.1:p.Phe115Ser
NM_001142806.1:c.-2T>C	NP_001136278.1:n.-2T>C
NM_005629.3:c.344T>C	NP_005620.1:p.Phe115Ser
NM_005629.4:c.344T>C MANE Select	NP_005620.1:p.Phe115Ser
NM_001142805.2:c.344T>C	NP_001136277.1:p.Phe115Ser