Canonical Allele Identifier: CA415076521

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153688725C>A , CM000685.2:g.153688725C>A GRCh38
NC_000023.10:g.152954180C>A , CM000685.1:g.152954180C>A GRCh37
NC_000023.9:g.152607374C>A NCBI36
NG_012016.1:g.5429C>A
NG_012016.2:g.5429C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000253122.10:c.151C>A (SLC6A8) MANE Select ENSP00000253122.5:p.Pro51Thr
ENST00000253122.9:c.151C>A (SLC6A8) ENSP00000253122.5:p.Pro51Thr
ENST00000458354.5:c.-3+90G>T (PNCK) ENSP00000401542.1:n.-3+90G>T
ENST00000476466.1:n.3C>A (SLC6A8)
ENST00000480693.1:n.64+90G>T (PNCK)
NM_001142805.1:c.151C>A (SLC6A8) NP_001136277.1:p.Pro51Thr
NM_005629.3:c.151C>A (SLC6A8) NP_005620.1:p.Pro51Thr
NM_005629.4:c.151C>A (SLC6A8) MANE Select NP_005620.1:p.Pro51Thr
NM_001142805.2:c.151C>A (SLC6A8) NP_001136277.1:p.Pro51Thr