Canonical Allele Identifier: CA382896318
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025307G>A , CM000673.2:g.119025307G>A GRCh38
NC_000011.9:g.118896017G>A , CM000673.1:g.118896017G>A GRCh37
NC_000011.8:g.118401227G>A NCBI36
NG_013331.1:g.10599C>T , LRG_187:g.10599C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.1217C>T (SLC37A4)
ENST00000697845.1:n.2206C>T (SLC37A4)
ENST00000697846.1:n.1579C>T (SLC37A4)
ENST00000697847.1:n.1290C>T (SLC37A4)
ENST00000697849.1:n.3683C>T (SLC37A4)
ENST00000697850.1:n.1874C>T (SLC37A4)
ENST00000697851.1:n.2845C>T (SLC37A4)
ENST00000638186.1:n.1311C>T (SLC37A4)
ENST00000638360.1:n.1143C>T (SLC37A4)
ENST00000638925.1:n.1276C>T (SLC37A4)
ENST00000650539.1:n.1479C>T (SLC37A4)
ENST00000330775.9:c.1007C>T (SLC37A4) ENSP00000476242.2:p.Ala336Val
ENST00000357590.9:c.1073C>T (SLC37A4) ENSP00000476176.2:p.Ala358Val
ENST00000524428.5:n.1243C>T (SLC37A4)
ENST00000525039.5:n.1497C>T (SLC37A4)
ENST00000525102.5:n.1765C>T (SLC37A4)
ENST00000525372.5:n.1105C>T (SLC37A4)
ENST00000526275.5:n.1789C>T (SLC37A4)
ENST00000527992.5:n.1235C>T (SLC37A4)
ENST00000529510.5:n.695C>T (SLC37A4)
ENST00000530407.5:n.1157C>T (SLC37A4)
ENST00000532085.1:n.5025C>T (SLC37A4)
ENST00000533058.5:c.*258G>A (TRAPPC4) ENSP00000432920.1:n.*258G>A
ENST00000538950.5:c.788C>T (SLC37A4) ENSP00000475991.2:p.Ala263Val
ENST00000545985.5:c.1007C>T (SLC37A4) ENSP00000475241.2:p.Ala336Val
NM_001164277.1:c.1007C>T , LRG_187t1:c.1007C>T (SLC37A4) NP_001157749.1:p.Ala336Val
NM_001164278.1:c.1073C>T (SLC37A4) NP_001157750.1:p.Ala358Val
NM_001164279.1:c.788C>T (SLC37A4) NP_001157751.1:p.Ala263Val
NM_001164280.1:c.1007C>T (SLC37A4) NP_001157752.1:p.Ala336Val
NM_001467.5:c.1007C>T (SLC37A4) NP_001458.1:p.Ala336Val
NM_001164278.2:c.1073C>T (SLC37A4) NP_001157750.1:p.Ala358Val
NM_001164279.2:c.788C>T (SLC37A4) NP_001157751.1:p.Ala263Val
NM_001164280.2:c.1007C>T (SLC37A4) NP_001157752.1:p.Ala336Val
NM_001467.6:c.1007C>T (SLC37A4) NP_001458.1:p.Ala336Val
NM_001164277.2:c.1007C>T (SLC37A4) MANE Select NP_001157749.1:p.Ala336Val