Canonical Allele Identifier: CA396938528
Gene: SLC38A8 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000299709.8:c.599A>T MANE Select ENSP00000299709.3:p.Gln200Leu
ENST00000299709.7:c.599A>T ENSP00000299709.3:p.Gln200Leu
ENST00000568178.1:c.599A>T ENSP00000457737.1:p.Gln200Leu
NM_001080442.2:c.599A>T NP_001073911.1:p.Gln200Leu
XM_011522872.1:c.599A>T XP_011521174.1:p.Gln200Leu
XM_017022946.1:c.599A>T XP_016878435.1:p.Gln200Leu
NM_001080442.3:c.599A>T MANE Select NP_001073911.1:p.Gln200Leu