Canonical Allele Identifier: CA2238382482

Gene: SLC38A8

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84032180_84032181delinsGT , CM000678.2:g.84032180_84032181delinsGT	GRCh38
NC_000016.9:g.84065785_84065786delinsGT , CM000678.1:g.84065785_84065786delinsGT	GRCh37
NC_000016.8:g.82623286_82623287delinsGT	NCBI36
NG_034136.1:g.14977_14978delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299709.8:c.531-213_531-212delinsAC MANE Select	ENSP00000299709.3:n.531-213_531-212delinsAC
ENST00000299709.7:c.531-213_531-212delinsAC	ENSP00000299709.3:n.531-213_531-212delinsAC
ENST00000568178.1:c.531-213_531-212delinsAC	ENSP00000457737.1:n.531-213_531-212delinsAC
NM_001080442.2:c.531-213_531-212delinsAC	NP_001073911.1:n.531-213_531-212delinsAC
XM_011522872.1:c.531-213_531-212delinsAC	XP_011521174.1:n.531-213_531-212delinsAC
XM_017022946.1:c.531-213_531-212delinsAC	XP_016878435.1:n.531-213_531-212delinsAC
NM_001080442.3:c.531-213_531-212delinsAC MANE Select	NP_001073911.1:n.531-213_531-212delinsAC