Canonical Allele Identifier: CA2807913793

Gene: SLC38A8

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84032191_84032201del , CM000678.2:g.84032191_84032201del	GRCh38
NC_000016.9:g.84065796_84065806del , CM000678.1:g.84065796_84065806del	GRCh37
NC_000016.8:g.82623297_82623307del	NCBI36
NG_034136.1:g.14958_14968del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299709.8:c.531-232_531-222del MANE Select	ENSP00000299709.3:n.531-232_531-222del
ENST00000299709.7:c.531-232_531-222del	ENSP00000299709.3:n.531-232_531-222del
ENST00000568178.1:c.531-232_531-222del	ENSP00000457737.1:n.531-232_531-222del
NM_001080442.2:c.531-232_531-222del	NP_001073911.1:n.531-232_531-222del
XM_011522872.1:c.531-232_531-222del	XP_011521174.1:n.531-232_531-222del
XM_017022946.1:c.531-232_531-222del	XP_016878435.1:n.531-232_531-222del
NM_001080442.3:c.531-232_531-222del MANE Select	NP_001073911.1:n.531-232_531-222del