Canonical Allele Identifier: CA415086984

Gene: SLC6A8

Linked Data

• MyVariant Identifiers: chrX:g.152959688T>C (hg19) ; chrX:g.153694233T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153694233T>C , CM000685.2:g.153694233T>C	GRCh38
NC_000023.10:g.152959688T>C , CM000685.1:g.152959688T>C	GRCh37
NC_000023.9:g.152612882T>C	NCBI36
NG_012016.1:g.10937T>C
NG_012016.2:g.10937T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.1358T>C MANE Select	ENSP00000253122.5:p.Leu453Pro
ENST00000253122.9:c.1358T>C	ENSP00000253122.5:p.Leu453Pro
ENST00000413787.1:c.287T>C	ENSP00000400463.1:p.Leu96Pro
ENST00000430077.6:c.1013T>C	ENSP00000403041.2:p.Leu338Pro
ENST00000442457.1:c.412T>C
ENST00000485324.1:n.1503T>C
NM_001142805.1:c.1328T>C	NP_001136277.1:p.Leu443Pro
NM_001142806.1:c.1013T>C	NP_001136278.1:p.Leu338Pro
NM_005629.3:c.1358T>C	NP_005620.1:p.Leu453Pro
NM_005629.4:c.1358T>C MANE Select	NP_005620.1:p.Leu453Pro
NM_001142805.2:c.1328T>C	NP_001136277.1:p.Leu443Pro