Canonical Allele Identifier: CA2238382627
Gene: SLC38A8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84032334G= , CM000678.2:g.84032334G= GRCh38
NC_000016.9:g.84065939G= , CM000678.1:g.84065939G= GRCh37
NC_000016.8:g.82623440G= NCBI36
NG_034136.1:g.14824C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299709.8:c.531-366C= MANE Select ENSP00000299709.3:n.531-366C=
ENST00000299709.7:c.531-366C= ENSP00000299709.3:n.531-366C=
ENST00000568178.1:c.531-366C= ENSP00000457737.1:n.531-366C=
NM_001080442.2:c.531-366C= NP_001073911.1:n.531-366C=
XM_011522872.1:c.531-366C= XP_011521174.1:n.531-366C=
XM_017022946.1:c.531-366C= XP_016878435.1:n.531-366C=
NM_001080442.3:c.531-366C= MANE Select NP_001073911.1:n.531-366C=
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