Canonical Allele Identifier: CA382902985
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119027765G>C , CM000673.2:g.119027765G>C GRCh38
NC_000011.9:g.118898475G>C , CM000673.1:g.118898475G>C GRCh37
NC_000011.8:g.118403685G>C NCBI36
NG_013331.1:g.8142C>G , LRG_187:g.8142C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.718C>G
ENST00000697845.1:n.642C>G
ENST00000697846.1:n.718C>G
ENST00000697847.1:n.718C>G
ENST00000697848.1:n.718C>G
ENST00000697849.1:n.1757C>G
ENST00000697850.1:n.718C>G
ENST00000697851.1:n.2078C>G
ENST00000638186.1:n.792C>G
ENST00000638360.1:n.624C>G
ENST00000638925.1:n.725C>G
ENST00000650539.1:n.894C>G
ENST00000330775.9:c.489C>G ENSP00000476242.2:p.Tyr163Ter
ENST00000357590.9:c.489C>G ENSP00000476176.2:p.Tyr163Ter
ENST00000524428.5:n.810C>G
ENST00000525039.5:n.912C>G
ENST00000525102.5:n.1246C>G
ENST00000525372.5:n.489C>G
ENST00000526275.5:n.1270C>G
ENST00000526626.6:n.451C>G
ENST00000527992.5:n.716C>G
ENST00000529510.5:n.399+429C>G
ENST00000530407.5:n.638C>G
ENST00000532085.1:n.3099C>G
ENST00000532888.6:n.784C>G
ENST00000538950.5:c.270C>G ENSP00000475991.2:p.Tyr90Ter
ENST00000545985.5:c.489C>G ENSP00000475241.2:p.Tyr163Ter
NM_001164277.1:c.489C>G , LRG_187t1:c.489C>G NP_001157749.1:p.Tyr163Ter
NM_001164278.1:c.489C>G NP_001157750.1:p.Tyr163Ter
NM_001164279.1:c.270C>G NP_001157751.1:p.Tyr90Ter
NM_001164280.1:c.489C>G NP_001157752.1:p.Tyr163Ter
NM_001467.5:c.489C>G NP_001458.1:p.Tyr163Ter
NM_001164278.2:c.489C>G NP_001157750.1:p.Tyr163Ter
NM_001164279.2:c.270C>G NP_001157751.1:p.Tyr90Ter
NM_001164280.2:c.489C>G NP_001157752.1:p.Tyr163Ter
NM_001467.6:c.489C>G NP_001458.1:p.Tyr163Ter
NM_001164277.2:c.489C>G MANE Select NP_001157749.1:p.Tyr163Ter