Canonical Allele Identifier: CA396938532
Gene: SLC38A8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84031900T>C , CM000678.2:g.84031900T>C GRCh38
NC_000016.9:g.84065505T>C , CM000678.1:g.84065505T>C GRCh37
NC_000016.8:g.82623006T>C NCBI36
NG_034136.1:g.15258A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299709.8:c.599A>G MANE Select ENSP00000299709.3:p.Gln200Arg
ENST00000299709.7:c.599A>G ENSP00000299709.3:p.Gln200Arg
ENST00000568178.1:c.599A>G ENSP00000457737.1:p.Gln200Arg
NM_001080442.2:c.599A>G NP_001073911.1:p.Gln200Arg
XM_011522872.1:c.599A>G XP_011521174.1:p.Gln200Arg
XM_017022946.1:c.599A>G XP_016878435.1:p.Gln200Arg
NM_001080442.3:c.599A>G MANE Select NP_001073911.1:p.Gln200Arg