Canonical Allele Identifier: CA2238382514

Gene: SLC38A8

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84032195_84032197delinsTTG , CM000678.2:g.84032195_84032197delinsTTG	GRCh38
NC_000016.9:g.84065800_84065802delinsTTG , CM000678.1:g.84065800_84065802delinsTTG	GRCh37
NC_000016.8:g.82623301_82623303delinsTTG	NCBI36
NG_034136.1:g.14961_14963delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299709.8:c.531-229_531-227delinsCAA MANE Select	ENSP00000299709.3:n.531-229_531-227delinsCAA
ENST00000299709.7:c.531-229_531-227delinsCAA	ENSP00000299709.3:n.531-229_531-227delinsCAA
ENST00000568178.1:c.531-229_531-227delinsCAA	ENSP00000457737.1:n.531-229_531-227delinsCAA
NM_001080442.2:c.531-229_531-227delinsCAA	NP_001073911.1:n.531-229_531-227delinsCAA
XM_011522872.1:c.531-229_531-227delinsCAA	XP_011521174.1:n.531-229_531-227delinsCAA
XM_017022946.1:c.531-229_531-227delinsCAA	XP_016878435.1:n.531-229_531-227delinsCAA
NM_001080442.3:c.531-229_531-227delinsCAA MANE Select	NP_001073911.1:n.531-229_531-227delinsCAA