Canonical Allele Identifier: CA382895914
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025267A>T , CM000673.2:g.119025267A>T GRCh38
NC_000011.9:g.118895977A>T , CM000673.1:g.118895977A>T GRCh37
NC_000011.8:g.118401187A>T NCBI36
NG_013331.1:g.10639T>A , LRG_187:g.10639T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1257T>A (SLC37A4)
ENST00000697845.1:n.2246T>A (SLC37A4)
ENST00000697846.1:n.1619T>A (SLC37A4)
ENST00000697847.1:n.1330T>A (SLC37A4)
ENST00000697849.1:n.3723T>A (SLC37A4)
ENST00000697850.1:n.1914T>A (SLC37A4)
ENST00000697851.1:n.2885T>A (SLC37A4)
ENST00000638186.1:n.1351T>A (SLC37A4)
ENST00000638360.1:n.1183T>A (SLC37A4)
ENST00000638925.1:n.1316T>A (SLC37A4)
ENST00000650539.1:n.1519T>A (SLC37A4)
ENST00000330775.9:c.1047T>A (SLC37A4) ENSP00000476242.2:p.Phe349Leu
ENST00000357590.9:c.1113T>A (SLC37A4) ENSP00000476176.2:p.Phe371Leu
ENST00000524428.5:n.1283T>A (SLC37A4)
ENST00000525039.5:n.1537T>A (SLC37A4)
ENST00000525102.5:n.1805T>A (SLC37A4)
ENST00000525372.5:n.1145T>A (SLC37A4)
ENST00000526275.5:n.1829T>A (SLC37A4)
ENST00000527992.5:n.1275T>A (SLC37A4)
ENST00000529510.5:n.735T>A (SLC37A4)
ENST00000530407.5:n.1197T>A (SLC37A4)
ENST00000532085.1:n.5065T>A (SLC37A4)
ENST00000533058.5:c.*218A>T (TRAPPC4) ENSP00000432920.1:n.*218A>T
ENST00000538950.5:c.828T>A (SLC37A4) ENSP00000475991.2:p.Phe276Leu
ENST00000545985.5:c.1047T>A (SLC37A4) ENSP00000475241.2:p.Phe349Leu
NM_001164277.1:c.1047T>A , LRG_187t1:c.1047T>A (SLC37A4) NP_001157749.1:p.Phe349Leu
NM_001164278.1:c.1113T>A (SLC37A4) NP_001157750.1:p.Phe371Leu
NM_001164279.1:c.828T>A (SLC37A4) NP_001157751.1:p.Phe276Leu
NM_001164280.1:c.1047T>A (SLC37A4) NP_001157752.1:p.Phe349Leu
NM_001467.5:c.1047T>A (SLC37A4) NP_001458.1:p.Phe349Leu
NM_001164278.2:c.1113T>A (SLC37A4) NP_001157750.1:p.Phe371Leu
NM_001164279.2:c.828T>A (SLC37A4) NP_001157751.1:p.Phe276Leu
NM_001164280.2:c.1047T>A (SLC37A4) NP_001157752.1:p.Phe349Leu
NM_001467.6:c.1047T>A (SLC37A4) NP_001458.1:p.Phe349Leu
NM_001164277.2:c.1047T>A (SLC37A4) MANE Select NP_001157749.1:p.Phe349Leu