Canonical Allele Identifier: CA519344918

Gene: SLC6A8

Linked Data

• MyVariant Identifiers: chrX:g.152959671G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153694216G>T , CM000685.2:g.153694216G>T	GRCh38
NC_000023.10:g.152959671G>T , CM000685.1:g.152959671G>T	GRCh37
NC_000023.9:g.152612865G>T	NCBI36
NG_012016.1:g.10920G>T
NG_012016.2:g.10920G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.1341G>T MANE Select	ENSP00000253122.5:p.Val447=
ENST00000253122.9:c.1341G>T	ENSP00000253122.5:p.Val447=
ENST00000413787.1:c.270G>T	ENSP00000400463.1:p.Val90=
ENST00000430077.6:c.996G>T	ENSP00000403041.2:p.Val332=
ENST00000442457.1:c.395G>T
ENST00000485324.1:n.1486G>T
NM_001142805.1:c.1311G>T	NP_001136277.1:p.Val437=
NM_001142806.1:c.996G>T	NP_001136278.1:p.Val332=
NM_005629.3:c.1341G>T	NP_005620.1:p.Val447=
NM_005629.4:c.1341G>T MANE Select	NP_005620.1:p.Val447=
NM_001142805.2:c.1311G>T	NP_001136277.1:p.Val437=