Canonical Allele Identifier: CA8200136
Gene: SLC38A8 HGNC NCBI

Linked Data

dbSNP Id: rs746835977
ExAC: 16:84065423 TGCCGTGCCTCCCC / T
gnomAD v2: 16-84065423-TGCCGTGCCTCCCC-T
MyVariant Identifiers: chr16:g.84065424_84065436del (hg19) chr16:g.84031819_84031831del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84031823_84031835del , CM000678.2:g.84031823_84031835del GRCh38
NC_000016.9:g.84065428_84065440del , CM000678.1:g.84065428_84065440del GRCh37
NC_000016.8:g.82622929_82622941del NCBI36
NG_034136.1:g.15327_15339del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299709.8:c.632+36_632+48del MANE Select ENSP00000299709.3:n.632+36_632+48del
ENST00000299709.7:c.632+36_632+48del ENSP00000299709.3:n.632+36_632+48del
ENST00000568178.1:c.632+36_632+48del ENSP00000457737.1:n.632+36_632+48del
NM_001080442.2:c.632+36_632+48del NP_001073911.1:n.632+36_632+48del
XM_011522872.1:c.632+36_632+48del XP_011521174.1:n.632+36_632+48del
XM_017022946.1:c.632+36_632+48del XP_016878435.1:n.632+36_632+48del
NM_001080442.3:c.632+36_632+48del MANE Select NP_001073911.1:n.632+36_632+48del
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