Canonical Allele Identifier: CA415076639

Linked Data

dbSNP Id: rs1557043846

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153688744G>T , CM000685.2:g.153688744G>T GRCh38
NC_000023.10:g.152954199G>T , CM000685.1:g.152954199G>T GRCh37
NC_000023.9:g.152607393G>T NCBI36
NG_012016.1:g.5448G>T
NG_012016.2:g.5448G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000253122.10:c.170G>T (SLC6A8) MANE Select ENSP00000253122.5:p.Arg57Leu
ENST00000253122.9:c.170G>T (SLC6A8) ENSP00000253122.5:p.Arg57Leu
ENST00000458354.5:c.-3+71C>A (PNCK) ENSP00000401542.1:n.-3+71C>A
ENST00000476466.1:n.22G>T (SLC6A8)
ENST00000480693.1:n.64+71C>A (PNCK)
NM_001142805.1:c.170G>T (SLC6A8) NP_001136277.1:p.Arg57Leu
NM_005629.3:c.170G>T (SLC6A8) NP_005620.1:p.Arg57Leu
NM_005629.4:c.170G>T (SLC6A8) MANE Select NP_005620.1:p.Arg57Leu
NM_001142805.2:c.170G>T (SLC6A8) NP_001136277.1:p.Arg57Leu