Canonical Allele Identifier: CA10549458

Gene: SLC6A8

Linked Data

• dbSNP Id: rs368884805
• ExAC: X:152959500 C / T
• gnomAD v2: X-152959500-C-T
• gnomAD v3: X-153694045-C-T
• gnomAD v4: X-153694045-C-T
• MyVariant Identifiers: chrX:g.152959500C>T (hg19) ; chrX:g.153694045C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153694045C>T , CM000685.2:g.153694045C>T	GRCh38
NC_000023.10:g.152959500C>T , CM000685.1:g.152959500C>T	GRCh37
NC_000023.9:g.152612694C>T	NCBI36
NG_012016.1:g.10749C>T
NG_012016.2:g.10749C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000253122.10:c.1254+28C>T MANE Select	ENSP00000253122.5:n.1254+28C>T
ENST00000253122.9:c.1254+28C>T	ENSP00000253122.5:n.1254+28C>T
ENST00000413787.1:c.258-159C>T	ENSP00000400463.1:n.258-159C>T
ENST00000430077.6:c.909+28C>T	ENSP00000403041.2:n.909+28C>T
ENST00000442457.1:c.308+28C>T
ENST00000457723.1:c.238+28C>T	ENSP00000394742.1:n.238+28C>T
ENST00000485324.1:n.1315C>T
NM_001142805.1:c.1224+28C>T	NP_001136277.1:n.1224+28C>T
NM_001142806.1:c.909+28C>T	NP_001136278.1:n.909+28C>T
NM_005629.3:c.1254+28C>T	NP_005620.1:n.1254+28C>T
NM_005629.4:c.1254+28C>T MANE Select	NP_005620.1:n.1254+28C>T
NM_001142805.2:c.1224+28C>T	NP_001136277.1:n.1224+28C>T