Canonical Allele Identifier: CA382896029
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025278T>A , CM000673.2:g.119025278T>A GRCh38
NC_000011.9:g.118895988T>A , CM000673.1:g.118895988T>A GRCh37
NC_000011.8:g.118401198T>A NCBI36
NG_013331.1:g.10628A>T , LRG_187:g.10628A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.1246A>T (SLC37A4)
ENST00000697845.1:n.2235A>T (SLC37A4)
ENST00000697846.1:n.1608A>T (SLC37A4)
ENST00000697847.1:n.1319A>T (SLC37A4)
ENST00000697849.1:n.3712A>T (SLC37A4)
ENST00000697850.1:n.1903A>T (SLC37A4)
ENST00000697851.1:n.2874A>T (SLC37A4)
ENST00000638186.1:n.1340A>T (SLC37A4)
ENST00000638360.1:n.1172A>T (SLC37A4)
ENST00000638925.1:n.1305A>T (SLC37A4)
ENST00000650539.1:n.1508A>T (SLC37A4)
ENST00000330775.9:c.1036A>T (SLC37A4) ENSP00000476242.2:p.Ile346Phe
ENST00000357590.9:c.1102A>T (SLC37A4) ENSP00000476176.2:p.Ile368Phe
ENST00000524428.5:n.1272A>T (SLC37A4)
ENST00000525039.5:n.1526A>T (SLC37A4)
ENST00000525102.5:n.1794A>T (SLC37A4)
ENST00000525372.5:n.1134A>T (SLC37A4)
ENST00000526275.5:n.1818A>T (SLC37A4)
ENST00000527992.5:n.1264A>T (SLC37A4)
ENST00000529510.5:n.724A>T (SLC37A4)
ENST00000530407.5:n.1186A>T (SLC37A4)
ENST00000532085.1:n.5054A>T (SLC37A4)
ENST00000533058.5:c.*229T>A (TRAPPC4) ENSP00000432920.1:n.*229T>A
ENST00000538950.5:c.817A>T (SLC37A4) ENSP00000475991.2:p.Ile273Phe
ENST00000545985.5:c.1036A>T (SLC37A4) ENSP00000475241.2:p.Ile346Phe
NM_001164277.1:c.1036A>T , LRG_187t1:c.1036A>T (SLC37A4) NP_001157749.1:p.Ile346Phe
NM_001164278.1:c.1102A>T (SLC37A4) NP_001157750.1:p.Ile368Phe
NM_001164279.1:c.817A>T (SLC37A4) NP_001157751.1:p.Ile273Phe
NM_001164280.1:c.1036A>T (SLC37A4) NP_001157752.1:p.Ile346Phe
NM_001467.5:c.1036A>T (SLC37A4) NP_001458.1:p.Ile346Phe
NM_001164278.2:c.1102A>T (SLC37A4) NP_001157750.1:p.Ile368Phe
NM_001164279.2:c.817A>T (SLC37A4) NP_001157751.1:p.Ile273Phe
NM_001164280.2:c.1036A>T (SLC37A4) NP_001157752.1:p.Ile346Phe
NM_001467.6:c.1036A>T (SLC37A4) NP_001458.1:p.Ile346Phe
NM_001164277.2:c.1036A>T (SLC37A4) MANE Select NP_001157749.1:p.Ile346Phe