Canonical Allele Identifier: CA415077910

Gene: SLC6A8

Linked Data

• MyVariant Identifiers: chrX:g.152955932A>C (hg19) ; chrX:g.153690477A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153690477A>C , CM000685.2:g.153690477A>C	GRCh38
NC_000023.10:g.152955932A>C , CM000685.1:g.152955932A>C	GRCh37
NC_000023.9:g.152609126A>C	NCBI36
NG_012016.1:g.7181A>C
NG_012016.2:g.7181A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.365A>C MANE Select	ENSP00000253122.5:p.Asn122Thr
ENST00000675713.1:n.119A>C
ENST00000253122.9:c.365A>C	ENSP00000253122.5:p.Asn122Thr
ENST00000430077.6:c.20A>C	ENSP00000403041.2:p.Asn7Thr
ENST00000476466.1:n.217A>C
NM_001142805.1:c.365A>C	NP_001136277.1:p.Asn122Thr
NM_001142806.1:c.20A>C	NP_001136278.1:p.Asn7Thr
NM_005629.3:c.365A>C	NP_005620.1:p.Asn122Thr
NM_005629.4:c.365A>C MANE Select	NP_005620.1:p.Asn122Thr
NM_001142805.2:c.365A>C	NP_001136277.1:p.Asn122Thr