Canonical Allele Identifier: CA2238382505

Gene: SLC38A8

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84032190_84032191delinsTG , CM000678.2:g.84032190_84032191delinsTG	GRCh38
NC_000016.9:g.84065795_84065796delinsTG , CM000678.1:g.84065795_84065796delinsTG	GRCh37
NC_000016.8:g.82623296_82623297delinsTG	NCBI36
NG_034136.1:g.14967_14968delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299709.8:c.531-223_531-222delinsCA MANE Select	ENSP00000299709.3:n.531-223_531-222delinsCA
ENST00000299709.7:c.531-223_531-222delinsCA	ENSP00000299709.3:n.531-223_531-222delinsCA
ENST00000568178.1:c.531-223_531-222delinsCA	ENSP00000457737.1:n.531-223_531-222delinsCA
NM_001080442.2:c.531-223_531-222delinsCA	NP_001073911.1:n.531-223_531-222delinsCA
XM_011522872.1:c.531-223_531-222delinsCA	XP_011521174.1:n.531-223_531-222delinsCA
XM_017022946.1:c.531-223_531-222delinsCA	XP_016878435.1:n.531-223_531-222delinsCA
NM_001080442.3:c.531-223_531-222delinsCA MANE Select	NP_001073911.1:n.531-223_531-222delinsCA