Canonical Allele Identifier: CA415086660

Gene: SLC6A8

Linked Data

• MyVariant Identifiers: chrX:g.152959585T>C (hg19) ; chrX:g.153694130T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153694130T>C , CM000685.2:g.153694130T>C	GRCh38
NC_000023.10:g.152959585T>C , CM000685.1:g.152959585T>C	GRCh37
NC_000023.9:g.152612779T>C	NCBI36
NG_012016.1:g.10834T>C
NG_012016.2:g.10834T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.1255T>C MANE Select	ENSP00000253122.5:p.Phe419Leu
ENST00000253122.9:c.1255T>C	ENSP00000253122.5:p.Phe419Leu
ENST00000413787.1:c.258-74T>C	ENSP00000400463.1:n.258-74T>C
ENST00000430077.6:c.910T>C	ENSP00000403041.2:p.Phe304Leu
ENST00000442457.1:c.309T>C
ENST00000457723.1:c.239-7T>C	ENSP00000394742.1:n.239-7T>C
ENST00000485324.1:n.1400T>C
NM_001142805.1:c.1225T>C	NP_001136277.1:p.Phe409Leu
NM_001142806.1:c.910T>C	NP_001136278.1:p.Phe304Leu
NM_005629.3:c.1255T>C	NP_005620.1:p.Phe419Leu
NM_005629.4:c.1255T>C MANE Select	NP_005620.1:p.Phe419Leu
NM_001142805.2:c.1225T>C	NP_001136277.1:p.Phe409Leu