Canonical Allele Identifier: CA8200137
Gene: SLC38A8 HGNC NCBI

Linked Data

dbSNP Id: rs746835977
ExAC: 16:84065423 T / TGCCGTGCCTCCCC
gnomAD v2: 16-84065423-T-TGCCGTGCCTCCCC
gnomAD v4: 16-84031818-T-TGCCGTGCCTCCCC
MyVariant Identifiers: chr16:g.84065436_84065437insGCCGTGCCTCCCC (hg19) chr16:g.84065423_84065424insGCCGTGCCTCCCC (hg19) chr16:g.84031818_84031819insGCCGTGCCTCCCC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.84031823_84031835dup , CM000678.2:g.84031823_84031835dup GRCh38
NC_000016.9:g.84065428_84065440dup , CM000678.1:g.84065428_84065440dup GRCh37
NC_000016.8:g.82622929_82622941dup NCBI36
NG_034136.1:g.15327_15339dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000299709.8:c.632+36_632+48dup MANE Select ENSP00000299709.3:n.632+36_632+48dup
ENST00000299709.7:c.632+36_632+48dup ENSP00000299709.3:n.632+36_632+48dup
ENST00000568178.1:c.632+36_632+48dup ENSP00000457737.1:n.632+36_632+48dup
NM_001080442.2:c.632+36_632+48dup NP_001073911.1:n.632+36_632+48dup
XM_011522872.1:c.632+36_632+48dup XP_011521174.1:n.632+36_632+48dup
XM_017022946.1:c.632+36_632+48dup XP_016878435.1:n.632+36_632+48dup
NM_001080442.3:c.632+36_632+48dup MANE Select NP_001073911.1:n.632+36_632+48dup
Search 100 bp 5'
Search 100 bp 3'