Canonical Allele Identifier: CA2634582861

Gene: SLC38A8

Linked Data

• gnomAD v4: 16-84032106-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84032108del , CM000678.2:g.84032108del	GRCh38
NC_000016.9:g.84065713del , CM000678.1:g.84065713del	GRCh37
NC_000016.8:g.82623214del	NCBI36
NG_034136.1:g.15051del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299709.8:c.531-139del MANE Select	ENSP00000299709.3:n.531-139del
ENST00000299709.7:c.531-139del	ENSP00000299709.3:n.531-139del
ENST00000568178.1:c.531-139del	ENSP00000457737.1:n.531-139del
NM_001080442.2:c.531-139del	NP_001073911.1:n.531-139del
XM_011522872.1:c.531-139del	XP_011521174.1:n.531-139del
XM_017022946.1:c.531-139del	XP_016878435.1:n.531-139del
NM_001080442.3:c.531-139del MANE Select	NP_001073911.1:n.531-139del