Canonical Allele Identifier: CA2238382145
Gene: SLC38A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84031795_84031808delinsAAGACTCCCCTCAC , CM000678.2:g.84031795_84031808delinsAAGACTCCCCTCAC GRCh38
NC_000016.9:g.84065400_84065413delinsAAGACTCCCCTCAC , CM000678.1:g.84065400_84065413delinsAAGACTCCCCTCAC GRCh37
NC_000016.8:g.82622901_82622914delinsAAGACTCCCCTCAC NCBI36
NG_034136.1:g.15350_15363delinsGTGAGGGGAGTCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000299709.8:c.632+59_632+72delinsGTGAGGGGAGTCTT MANE Select ENSP00000299709.3:n.632+59_632+72delinsGT...
ENST00000299709.7:c.632+59_632+72delinsGTGAGGGGAGTCTT ENSP00000299709.3:n.632+59_632+72delinsGT...
ENST00000568178.1:c.632+59_632+72delinsGTGAGGGGAGTCTT ENSP00000457737.1:n.632+59_632+72delinsGT...
NM_001080442.2:c.632+59_632+72delinsGTGAGGGGAGTCTT NP_001073911.1:n.632+59_632+72delinsGTGAG...
XM_011522872.1:c.632+59_632+72delinsGTGAGGGGAGTCTT XP_011521174.1:n.632+59_632+72delinsGTGAG...
XM_017022946.1:c.632+59_632+72delinsGTGAGGGGAGTCTT XP_016878435.1:n.632+59_632+72delinsGTGAG...
NM_001080442.3:c.632+59_632+72delinsGTGAGGGGAGTCTT MANE Select NP_001073911.1:n.632+59_632+72delinsGTGAG...