Canonical Allele Identifier: CA285457538

Gene: SLC38A8

Linked Data

• dbSNP Id: rs386793317

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84032172_84032188delinsGTT , CM000678.2:g.84032172_84032188delinsGTT	GRCh38
NC_000016.9:g.84065777_84065793delinsGTT , CM000678.1:g.84065777_84065793delinsGTT	GRCh37
NC_000016.8:g.82623278_82623294delinsGTT	NCBI36
NG_034136.1:g.14970_14986delinsAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299709.8:c.531-220_531-204delinsAAC MANE Select	ENSP00000299709.3:n.531-220_531-204delinsAAC
ENST00000299709.7:c.531-220_531-204delinsAAC	ENSP00000299709.3:n.531-220_531-204delinsAAC
ENST00000568178.1:c.531-220_531-204delinsAAC	ENSP00000457737.1:n.531-220_531-204delinsAAC
NM_001080442.2:c.531-220_531-204delinsAAC	NP_001073911.1:n.531-220_531-204delinsAAC
XM_011522872.1:c.531-220_531-204delinsAAC	XP_011521174.1:n.531-220_531-204delinsAAC
XM_017022946.1:c.531-220_531-204delinsAAC	XP_016878435.1:n.531-220_531-204delinsAAC
NM_001080442.3:c.531-220_531-204delinsAAC MANE Select	NP_001073911.1:n.531-220_531-204delinsAAC