Canonical Allele Identifier: CA725007630
Gene: SLC38A8 HGNC NCBI

Linked Data

dbSNP Id: rs1328979324

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84031806_84031818del , CM000678.2:g.84031806_84031818del GRCh38
NC_000016.9:g.84065411_84065423del , CM000678.1:g.84065411_84065423del GRCh37
NC_000016.8:g.82622912_82622924del NCBI36
NG_034136.1:g.15350_15362del

Transcript Alleles

HGVS Amino-acid change
ENST00000299709.8:c.632+59_632+71del MANE Select ENSP00000299709.3:n.632+59_632+71del
ENST00000299709.7:c.632+59_632+71del ENSP00000299709.3:n.632+59_632+71del
ENST00000568178.1:c.632+59_632+71del ENSP00000457737.1:n.632+59_632+71del
NM_001080442.2:c.632+59_632+71del NP_001073911.1:n.632+59_632+71del
XM_011522872.1:c.632+59_632+71del XP_011521174.1:n.632+59_632+71del
XM_017022946.1:c.632+59_632+71del XP_016878435.1:n.632+59_632+71del
NM_001080442.3:c.632+59_632+71del MANE Select NP_001073911.1:n.632+59_632+71del