Canonical Allele Identifier: CA2238382455

Gene: SLC38A8

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84032169_84032182delinsGTTTTGTTGTTGTT , CM000678.2:g.84032169_84032182delinsGTTTTGTTGTTGTT	GRCh38
NC_000016.9:g.84065774_84065787delinsGTTTTGTTGTTGTT , CM000678.1:g.84065774_84065787delinsGTTTTGTTGTTGTT	GRCh37
NC_000016.8:g.82623275_82623288delinsGTTTTGTTGTTGTT	NCBI36
NG_034136.1:g.14976_14989delinsAACAACAACAAAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299709.8:c.531-214_531-201delinsAACAACAACAAAAC MANE Select	ENSP00000299709.3:n.531-214_531-201delinsAACAACAACAAAAC
ENST00000299709.7:c.531-214_531-201delinsAACAACAACAAAAC	ENSP00000299709.3:n.531-214_531-201delinsAACAACAACAAAAC
ENST00000568178.1:c.531-214_531-201delinsAACAACAACAAAAC	ENSP00000457737.1:n.531-214_531-201delinsAACAACAACAAAAC
NM_001080442.2:c.531-214_531-201delinsAACAACAACAAAAC	NP_001073911.1:n.531-214_531-201delinsAACAACAACAAAAC
XM_011522872.1:c.531-214_531-201delinsAACAACAACAAAAC	XP_011521174.1:n.531-214_531-201delinsAACAACAACAAAAC
XM_017022946.1:c.531-214_531-201delinsAACAACAACAAAAC	XP_016878435.1:n.531-214_531-201delinsAACAACAACAAAAC
NM_001080442.3:c.531-214_531-201delinsAACAACAACAAAAC MANE Select	NP_001073911.1:n.531-214_531-201delinsAACAACAACAAAAC