Canonical Allele Identifier: CA2238382414

Gene: SLC38A8

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84032129_84032130delinsTG , CM000678.2:g.84032129_84032130delinsTG	GRCh38
NC_000016.9:g.84065734_84065735delinsTG , CM000678.1:g.84065734_84065735delinsTG	GRCh37
NC_000016.8:g.82623235_82623236delinsTG	NCBI36
NG_034136.1:g.15028_15029delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299709.8:c.531-162_531-161delinsCA MANE Select	ENSP00000299709.3:n.531-162_531-161delinsCA
ENST00000299709.7:c.531-162_531-161delinsCA	ENSP00000299709.3:n.531-162_531-161delinsCA
ENST00000568178.1:c.531-162_531-161delinsCA	ENSP00000457737.1:n.531-162_531-161delinsCA
NM_001080442.2:c.531-162_531-161delinsCA	NP_001073911.1:n.531-162_531-161delinsCA
XM_011522872.1:c.531-162_531-161delinsCA	XP_011521174.1:n.531-162_531-161delinsCA
XM_017022946.1:c.531-162_531-161delinsCA	XP_016878435.1:n.531-162_531-161delinsCA
NM_001080442.3:c.531-162_531-161delinsCA MANE Select	NP_001073911.1:n.531-162_531-161delinsCA