Canonical Allele Identifier: CA2238382517

Gene: SLC38A8

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84032198_84032200delinsTTG , CM000678.2:g.84032198_84032200delinsTTG	GRCh38
NC_000016.9:g.84065803_84065805delinsTTG , CM000678.1:g.84065803_84065805delinsTTG	GRCh37
NC_000016.8:g.82623304_82623306delinsTTG	NCBI36
NG_034136.1:g.14958_14960delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299709.8:c.531-232_531-230delinsCAA MANE Select	ENSP00000299709.3:n.531-232_531-230delinsCAA
ENST00000299709.7:c.531-232_531-230delinsCAA	ENSP00000299709.3:n.531-232_531-230delinsCAA
ENST00000568178.1:c.531-232_531-230delinsCAA	ENSP00000457737.1:n.531-232_531-230delinsCAA
NM_001080442.2:c.531-232_531-230delinsCAA	NP_001073911.1:n.531-232_531-230delinsCAA
XM_011522872.1:c.531-232_531-230delinsCAA	XP_011521174.1:n.531-232_531-230delinsCAA
XM_017022946.1:c.531-232_531-230delinsCAA	XP_016878435.1:n.531-232_531-230delinsCAA
NM_001080442.3:c.531-232_531-230delinsCAA MANE Select	NP_001073911.1:n.531-232_531-230delinsCAA