Canonical Allele Identifier: CA2238382585

Gene: SLC38A8

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84032281_84032282delinsCG , CM000678.2:g.84032281_84032282delinsCG	GRCh38
NC_000016.9:g.84065886_84065887delinsCG , CM000678.1:g.84065886_84065887delinsCG	GRCh37
NC_000016.8:g.82623387_82623388delinsCG	NCBI36
NG_034136.1:g.14876_14877delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299709.8:c.531-314_531-313delinsCG MANE Select	ENSP00000299709.3:n.531-314_531-313delinsCG
ENST00000299709.7:c.531-314_531-313delinsCG	ENSP00000299709.3:n.531-314_531-313delinsCG
ENST00000568178.1:c.531-314_531-313delinsCG	ENSP00000457737.1:n.531-314_531-313delinsCG
NM_001080442.2:c.531-314_531-313delinsCG	NP_001073911.1:n.531-314_531-313delinsCG
XM_011522872.1:c.531-314_531-313delinsCG	XP_011521174.1:n.531-314_531-313delinsCG
XM_017022946.1:c.531-314_531-313delinsCG	XP_016878435.1:n.531-314_531-313delinsCG
NM_001080442.3:c.531-314_531-313delinsCG MANE Select	NP_001073911.1:n.531-314_531-313delinsCG