Canonical Allele Identifier: CA2634582695
Gene: SLC38A8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84031804dup , CM000678.2:g.84031804dup GRCh38
NC_000016.9:g.84065409dup , CM000678.1:g.84065409dup GRCh37
NC_000016.8:g.82622910dup NCBI36
NG_034136.1:g.15357dup

Transcript Alleles

HGVS Amino-acid change
ENST00000299709.8:c.632+66dup MANE Select ENSP00000299709.3:n.632+66dup
ENST00000299709.7:c.632+66dup ENSP00000299709.3:n.632+66dup
ENST00000568178.1:c.632+66dup ENSP00000457737.1:n.632+66dup
NM_001080442.2:c.632+66dup NP_001073911.1:n.632+66dup
XM_011522872.1:c.632+66dup XP_011521174.1:n.632+66dup
XM_017022946.1:c.632+66dup XP_016878435.1:n.632+66dup
NM_001080442.3:c.632+66dup MANE Select NP_001073911.1:n.632+66dup