Canonical Allele Identifier: CA2634582729
Gene: SLC38A8 HGNC NCBI

Linked Data

dbSNP Id: rs2151124896

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84031878del , CM000678.2:g.84031878del GRCh38
NC_000016.9:g.84065483del , CM000678.1:g.84065483del GRCh37
NC_000016.8:g.82622984del NCBI36
NG_034136.1:g.15280del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299709.8:c.621del MANE Select ENSP00000299709.3:p.Pro208LeufsTer3
ENST00000299709.7:c.621del ENSP00000299709.3:p.Pro208LeufsTer3
ENST00000568178.1:c.621del ENSP00000457737.1:p.Pro208LeufsTer3
NM_001080442.2:c.621del NP_001073911.1:p.Pro208LeufsTer3
XM_011522872.1:c.621del XP_011521174.1:p.Pro208LeufsTer3
XM_017022946.1:c.621del XP_016878435.1:p.Pro208LeufsTer3
NM_001080442.3:c.621del MANE Select NP_001073911.1:p.Pro208LeufsTer3