Canonical Allele Identifier: CA2841147236
Gene: SLC38A8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84031813del , CM000678.2:g.84031813del GRCh38
NC_000016.9:g.84065418del , CM000678.1:g.84065418del GRCh37
NC_000016.8:g.82622919del NCBI36
NG_034136.1:g.15345del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299709.8:c.632+54del MANE Select ENSP00000299709.3:n.632+54del
ENST00000299709.7:c.632+54del ENSP00000299709.3:n.632+54del
ENST00000568178.1:c.632+54del ENSP00000457737.1:n.632+54del
NM_001080442.2:c.632+54del NP_001073911.1:n.632+54del
XM_011522872.1:c.632+54del XP_011521174.1:n.632+54del
XM_017022946.1:c.632+54del XP_016878435.1:n.632+54del
NM_001080442.3:c.632+54del MANE Select NP_001073911.1:n.632+54del
Search 100 bp 5'
Search 100 bp 3'