Canonical Allele Identifier: CA2466435979
Gene: SLC6A8 HGNC NCBI
PNCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153688903G= , CM000685.2:g.153688903G= GRCh38
NC_000023.10:g.152954358G= , CM000685.1:g.152954358G= GRCh37
NC_000023.9:g.152607552G= NCBI36
NG_012016.1:g.5607G=
NG_012016.2:g.5607G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253122.10:c.262+67G= (SLC6A8) MANE Select ENSP00000253122.5:n.262+67G=
ENST00000253122.9:c.262+67G= (SLC6A8) ENSP00000253122.5:n.262+67G=
ENST00000458354.5:c.-91C= (PNCK) ENSP00000401542.1:n.-91C=
ENST00000476466.1:n.114+67G= (SLC6A8)
NM_001142805.1:c.262+67G= (SLC6A8) NP_001136277.1:n.262+67G=
NM_005629.3:c.262+67G= (SLC6A8) NP_005620.1:n.262+67G=
NM_005629.4:c.262+67G= (SLC6A8) MANE Select NP_005620.1:n.262+67G=
NM_001142805.2:c.262+67G= (SLC6A8) NP_001136277.1:n.262+67G=
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