Canonical Allele Identifier: CA2238382486

Gene: SLC38A8

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84032183_84032186delinsGTTT , CM000678.2:g.84032183_84032186delinsGTTT	GRCh38
NC_000016.9:g.84065788_84065791delinsGTTT , CM000678.1:g.84065788_84065791delinsGTTT	GRCh37
NC_000016.8:g.82623289_82623292delinsGTTT	NCBI36
NG_034136.1:g.14972_14975delinsAAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299709.8:c.531-218_531-215delinsAAAC MANE Select	ENSP00000299709.3:n.531-218_531-215delinsAAAC
ENST00000299709.7:c.531-218_531-215delinsAAAC	ENSP00000299709.3:n.531-218_531-215delinsAAAC
ENST00000568178.1:c.531-218_531-215delinsAAAC	ENSP00000457737.1:n.531-218_531-215delinsAAAC
NM_001080442.2:c.531-218_531-215delinsAAAC	NP_001073911.1:n.531-218_531-215delinsAAAC
XM_011522872.1:c.531-218_531-215delinsAAAC	XP_011521174.1:n.531-218_531-215delinsAAAC
XM_017022946.1:c.531-218_531-215delinsAAAC	XP_016878435.1:n.531-218_531-215delinsAAAC
NM_001080442.3:c.531-218_531-215delinsAAAC MANE Select	NP_001073911.1:n.531-218_531-215delinsAAAC