Canonical Allele Identifier: CA285457154
Gene: SLC38A8 HGNC NCBI

Linked Data

dbSNP Id: rs930213649

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84031922C>T , CM000678.2:g.84031922C>T GRCh38
NC_000016.9:g.84065527C>T , CM000678.1:g.84065527C>T GRCh37
NC_000016.8:g.82623028C>T NCBI36
NG_034136.1:g.15236G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299709.8:c.577G>A MANE Select ENSP00000299709.3:p.Val193Met
ENST00000299709.7:c.577G>A ENSP00000299709.3:p.Val193Met
ENST00000568178.1:c.577G>A ENSP00000457737.1:p.Val193Met
NM_001080442.2:c.577G>A NP_001073911.1:p.Val193Met
XM_011522872.1:c.577G>A XP_011521174.1:p.Val193Met
XM_017022946.1:c.577G>A XP_016878435.1:p.Val193Met
NM_001080442.3:c.577G>A MANE Select NP_001073911.1:p.Val193Met