Canonical Allele Identifier: CA2238382490

Gene: SLC38A8

Linked Data

• dbSNP Id: rs1555555487

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84032186_84032187del , CM000678.2:g.84032186_84032187del	GRCh38
NC_000016.9:g.84065791_84065792del , CM000678.1:g.84065791_84065792del	GRCh37
NC_000016.8:g.82623292_82623293del	NCBI36
NG_034136.1:g.14973_14974del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299709.8:c.531-217_531-216del MANE Select	ENSP00000299709.3:n.531-217_531-216del
ENST00000299709.7:c.531-217_531-216del	ENSP00000299709.3:n.531-217_531-216del
ENST00000568178.1:c.531-217_531-216del	ENSP00000457737.1:n.531-217_531-216del
NM_001080442.2:c.531-217_531-216del	NP_001073911.1:n.531-217_531-216del
XM_011522872.1:c.531-217_531-216del	XP_011521174.1:n.531-217_531-216del
XM_017022946.1:c.531-217_531-216del	XP_016878435.1:n.531-217_531-216del
NM_001080442.3:c.531-217_531-216del MANE Select	NP_001073911.1:n.531-217_531-216del