Canonical Allele Identifier: CA2238382493

Gene: SLC38A8

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84032186_84032188delinsTTG , CM000678.2:g.84032186_84032188delinsTTG	GRCh38
NC_000016.9:g.84065791_84065793delinsTTG , CM000678.1:g.84065791_84065793delinsTTG	GRCh37
NC_000016.8:g.82623292_82623294delinsTTG	NCBI36
NG_034136.1:g.14970_14972delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299709.8:c.531-220_531-218delinsCAA MANE Select	ENSP00000299709.3:n.531-220_531-218delinsCAA
ENST00000299709.7:c.531-220_531-218delinsCAA	ENSP00000299709.3:n.531-220_531-218delinsCAA
ENST00000568178.1:c.531-220_531-218delinsCAA	ENSP00000457737.1:n.531-220_531-218delinsCAA
NM_001080442.2:c.531-220_531-218delinsCAA	NP_001073911.1:n.531-220_531-218delinsCAA
XM_011522872.1:c.531-220_531-218delinsCAA	XP_011521174.1:n.531-220_531-218delinsCAA
XM_017022946.1:c.531-220_531-218delinsCAA	XP_016878435.1:n.531-220_531-218delinsCAA
NM_001080442.3:c.531-220_531-218delinsCAA MANE Select	NP_001073911.1:n.531-220_531-218delinsCAA