Canonical Allele Identifier: CA415076471

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153688717C>A , CM000685.2:g.153688717C>A GRCh38
NC_000023.10:g.152954172C>A , CM000685.1:g.152954172C>A GRCh37
NC_000023.9:g.152607366C>A NCBI36
NG_012016.1:g.5421C>A
NG_012016.2:g.5421C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000253122.10:c.143C>A (SLC6A8) MANE Select ENSP00000253122.5:p.Ala48Asp
ENST00000253122.9:c.143C>A (SLC6A8) ENSP00000253122.5:p.Ala48Asp
ENST00000458354.5:c.-3+98G>T (PNCK) ENSP00000401542.1:n.-3+98G>T
ENST00000480693.1:n.64+98G>T (PNCK)
NM_001142805.1:c.143C>A (SLC6A8) NP_001136277.1:p.Ala48Asp
NM_005629.3:c.143C>A (SLC6A8) NP_005620.1:p.Ala48Asp
NM_005629.4:c.143C>A (SLC6A8) MANE Select NP_005620.1:p.Ala48Asp
NM_001142805.2:c.143C>A (SLC6A8) NP_001136277.1:p.Ala48Asp