Canonical Allele Identifier: CA2466437833
Community Standard Title: NM_005629.4(SLC6A8):c.1011C= (p.Cys337=)
Gene: SLC6A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153693361C= , CM000685.2:g.153693361C= GRCh38
NC_000023.10:g.152958816C= , CM000685.1:g.152958816C= GRCh37
NC_000023.9:g.152612010C= NCBI36
NG_012016.1:g.10065C=
NG_012016.2:g.10065C=

Transcript Alleles

HGVS Amino-acid Change
NM_005629.4:c.1011C= MANE Select NP_005620.1:p.Cys337=
ENST00000253122.10:c.1011C= MANE Select ENSP00000253122.5:p.Cys337=
NM_001142805.1:c.1011C= NP_001136277.1:p.Cys337=
NM_001142805.2:c.1011C= NP_001136277.1:p.Cys337=
NM_001142806.1:c.666C= NP_001136278.1:p.Cys222=
NM_005629.3:c.1011C= NP_005620.1:p.Cys337=
ENST00000253122.9:c.1011C= ENSP00000253122.5:p.Cys337=
ENST00000413787.1:c.157C= ENSP00000400463.1:p.Leu53=
ENST00000430077.6:c.666C= ENSP00000403041.2:p.Cys222=
ENST00000442457.1:c.95C=
ENST00000467402.1:n.146-131C=
ENST00000485324.1:n.1044C=