Canonical Allele Identifier: CA415086752
Gene: SLC6A8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153694170T>C , CM000685.2:g.153694170T>C GRCh38
NC_000023.10:g.152959625T>C , CM000685.1:g.152959625T>C GRCh37
NC_000023.9:g.152612819T>C NCBI36
NG_012016.1:g.10874T>C
NG_012016.2:g.10874T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000253122.10:c.1295T>C MANE Select ENSP00000253122.5:p.Leu432Pro
ENST00000253122.9:c.1295T>C ENSP00000253122.5:p.Leu432Pro
ENST00000413787.1:c.258-34T>C ENSP00000400463.1:n.258-34T>C
ENST00000430077.6:c.950T>C ENSP00000403041.2:p.Leu317Pro
ENST00000442457.1:c.349T>C
ENST00000485324.1:n.1440T>C
NM_001142805.1:c.1265T>C NP_001136277.1:p.Leu422Pro
NM_001142806.1:c.950T>C NP_001136278.1:p.Leu317Pro
NM_005629.3:c.1295T>C NP_005620.1:p.Leu432Pro
NM_005629.4:c.1295T>C MANE Select NP_005620.1:p.Leu432Pro
NM_001142805.2:c.1265T>C NP_001136277.1:p.Leu422Pro