Canonical Allele Identifier: CA2599859100
Gene: SLC38A8 HGNC NCBI

Linked Data

gnomAD v3: 16-84032298-C-A
gnomAD v4: 16-84032298-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84032298C>A , CM000678.2:g.84032298C>A GRCh38
NC_000016.9:g.84065903C>A , CM000678.1:g.84065903C>A GRCh37
NC_000016.8:g.82623404C>A NCBI36
NG_034136.1:g.14860G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299709.8:c.531-330G>T MANE Select ENSP00000299709.3:n.531-330G>T
ENST00000299709.7:c.531-330G>T ENSP00000299709.3:n.531-330G>T
ENST00000568178.1:c.531-330G>T ENSP00000457737.1:n.531-330G>T
NM_001080442.2:c.531-330G>T NP_001073911.1:n.531-330G>T
XM_011522872.1:c.531-330G>T XP_011521174.1:n.531-330G>T
XM_017022946.1:c.531-330G>T XP_016878435.1:n.531-330G>T
NM_001080442.3:c.531-330G>T MANE Select NP_001073911.1:n.531-330G>T
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