Canonical Allele Identifier: CA477367264
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.118895920A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025210A>T , CM000673.2:g.119025210A>T GRCh38
NC_000011.9:g.118895920A>T , CM000673.1:g.118895920A>T GRCh37
NC_000011.8:g.118401130A>T NCBI36
NG_013331.1:g.10696T>A , LRG_187:g.10696T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1314T>A (SLC37A4)
ENST00000697845.1:n.2303T>A (SLC37A4)
ENST00000697846.1:n.1676T>A (SLC37A4)
ENST00000697847.1:n.1387T>A (SLC37A4)
ENST00000697849.1:n.3780T>A (SLC37A4)
ENST00000697850.1:n.1971T>A (SLC37A4)
ENST00000697851.1:n.2942T>A (SLC37A4)
ENST00000638186.1:n.1408T>A (SLC37A4)
ENST00000638360.1:n.1240T>A (SLC37A4)
ENST00000638925.1:n.1373T>A (SLC37A4)
ENST00000650539.1:n.1576T>A (SLC37A4)
ENST00000330775.9:c.1104T>A (SLC37A4) ENSP00000476242.2:p.Ile368=
ENST00000357590.9:c.1170T>A (SLC37A4) ENSP00000476176.2:p.Ile390=
ENST00000524428.5:n.1340T>A (SLC37A4)
ENST00000525039.5:n.1594T>A (SLC37A4)
ENST00000525102.5:n.1862T>A (SLC37A4)
ENST00000525372.5:n.1202T>A (SLC37A4)
ENST00000526275.5:n.1886T>A (SLC37A4)
ENST00000527992.5:n.1332T>A (SLC37A4)
ENST00000529510.5:n.792T>A (SLC37A4)
ENST00000530407.5:n.1254T>A (SLC37A4)
ENST00000532085.1:n.5122T>A (SLC37A4)
ENST00000533058.5:c.*161A>T (TRAPPC4) ENSP00000432920.1:n.*161A>T
ENST00000538950.5:c.885T>A (SLC37A4) ENSP00000475991.2:p.Ile295=
ENST00000545985.5:c.1104T>A (SLC37A4) ENSP00000475241.2:p.Ile368=
NM_001164277.1:c.1104T>A , LRG_187t1:c.1104T>A (SLC37A4) NP_001157749.1:p.Ile368=
NM_001164278.1:c.1170T>A (SLC37A4) NP_001157750.1:p.Ile390=
NM_001164279.1:c.885T>A (SLC37A4) NP_001157751.1:p.Ile295=
NM_001164280.1:c.1104T>A (SLC37A4) NP_001157752.1:p.Ile368=
NM_001467.5:c.1104T>A (SLC37A4) NP_001458.1:p.Ile368=
NM_001164278.2:c.1170T>A (SLC37A4) NP_001157750.1:p.Ile390=
NM_001164279.2:c.885T>A (SLC37A4) NP_001157751.1:p.Ile295=
NM_001164280.2:c.1104T>A (SLC37A4) NP_001157752.1:p.Ile368=
NM_001467.6:c.1104T>A (SLC37A4) NP_001458.1:p.Ile368=
NM_001164277.2:c.1104T>A (SLC37A4) MANE Select NP_001157749.1:p.Ile368=