Canonical Allele Identifier: CA2634582728
Gene: SLC38A8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84031866_84031870del , CM000678.2:g.84031866_84031870del GRCh38
NC_000016.9:g.84065471_84065475del , CM000678.1:g.84065471_84065475del GRCh37
NC_000016.8:g.82622972_82622976del NCBI36
NG_034136.1:g.15289_15293del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299709.8:c.630_632+2del
ENST00000299709.7:c.630_632+2del
ENST00000568178.1:c.630_632+2del
NM_001080442.2:c.630_632+2del
XM_011522872.1:c.630_632+2del
XM_017022946.1:c.630_632+2del
NM_001080442.3:c.630_632+2del