Canonical Allele Identifier: CA396938661
Gene: SLC38A8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84031919G>T , CM000678.2:g.84031919G>T GRCh38
NC_000016.9:g.84065524G>T , CM000678.1:g.84065524G>T GRCh37
NC_000016.8:g.82623025G>T NCBI36
NG_034136.1:g.15239C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299709.8:c.580C>A MANE Select ENSP00000299709.3:p.Gln194Lys
ENST00000299709.7:c.580C>A ENSP00000299709.3:p.Gln194Lys
ENST00000568178.1:c.580C>A ENSP00000457737.1:p.Gln194Lys
NM_001080442.2:c.580C>A NP_001073911.1:p.Gln194Lys
XM_011522872.1:c.580C>A XP_011521174.1:p.Gln194Lys
XM_017022946.1:c.580C>A XP_016878435.1:p.Gln194Lys
NM_001080442.3:c.580C>A MANE Select NP_001073911.1:p.Gln194Lys