Canonical Allele Identifier: CA2238382483

Gene: SLC38A8

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84032181_84032200delinsTTGTTTTGTTGTTGTTGTTG , CM000678.2:g.84032181_84032200delinsTTGTTTTGTTGTTGTTGTTG	GRCh38
NC_000016.9:g.84065786_84065805delinsTTGTTTTGTTGTTGTTGTTG , CM000678.1:g.84065786_84065805delinsTTGTTTTGTTGTTGTTGTTG	GRCh37
NC_000016.8:g.82623287_82623306delinsTTGTTTTGTTGTTGTTGTTG	NCBI36
NG_034136.1:g.14958_14977delinsCAACAACAACAACAAAACAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299709.8:c.531-232_531-213delinsCAACAACAACAACAAAACAA MANE Select	ENSP00000299709.3:n.531-232_531-213delinsCAACAACAACAACAAAACAA...
ENST00000299709.7:c.531-232_531-213delinsCAACAACAACAACAAAACAA	ENSP00000299709.3:n.531-232_531-213delinsCAACAACAACAACAAAACAA...
ENST00000568178.1:c.531-232_531-213delinsCAACAACAACAACAAAACAA	ENSP00000457737.1:n.531-232_531-213delinsCAACAACAACAACAAAACAA...
NM_001080442.2:c.531-232_531-213delinsCAACAACAACAACAAAACAA	NP_001073911.1:n.531-232_531-213delinsCAACAACAACAACAAAACAA
XM_011522872.1:c.531-232_531-213delinsCAACAACAACAACAAAACAA	XP_011521174.1:n.531-232_531-213delinsCAACAACAACAACAAAACAA
XM_017022946.1:c.531-232_531-213delinsCAACAACAACAACAAAACAA	XP_016878435.1:n.531-232_531-213delinsCAACAACAACAACAAAACAA
NM_001080442.3:c.531-232_531-213delinsCAACAACAACAACAAAACAA MANE Select	NP_001073911.1:n.531-232_531-213delinsCAACAACAACAACAAAACAA