Canonical Allele Identifier: CA2003748238
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119024914T= , CM000673.2:g.119024914T= GRCh38
NC_000011.9:g.118895624T= , CM000673.1:g.118895624T= GRCh37
NC_000011.8:g.118400834T= NCBI36
NG_013331.1:g.10992A= , LRG_187:g.10992A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1496A= (SLC37A4)
ENST00000697845.1:n.2485A= (SLC37A4)
ENST00000697846.1:n.1858A= (SLC37A4)
ENST00000697847.1:n.1569A= (SLC37A4)
ENST00000697849.1:n.3962A= (SLC37A4)
ENST00000697850.1:n.2153A= (SLC37A4)
ENST00000697851.1:n.3124A= (SLC37A4)
ENST00000638186.1:n.1590A= (SLC37A4)
ENST00000638360.1:n.1422A= (SLC37A4)
ENST00000638925.1:n.1555A= (SLC37A4)
ENST00000650539.1:n.1758A= (SLC37A4)
ENST00000330775.9:c.1286A= (SLC37A4) ENSP00000476242.2:p.Glu429=
ENST00000357590.9:c.1352A= (SLC37A4) ENSP00000476176.2:p.Glu451=
ENST00000524428.5:n.1522A= (SLC37A4)
ENST00000525039.5:n.1776A= (SLC37A4)
ENST00000525102.5:n.2044A= (SLC37A4)
ENST00000525372.5:n.1384A= (SLC37A4)
ENST00000526275.5:n.2068A= (SLC37A4)
ENST00000527992.5:n.1514A= (SLC37A4)
ENST00000530407.5:n.1436A= (SLC37A4)
ENST00000532085.1:n.5304A= (SLC37A4)
ENST00000533058.5:c.639T= (TRAPPC4) ENSP00000432920.1:p.Thr213=
ENST00000538950.5:c.1067A= (SLC37A4) ENSP00000475991.2:p.Glu356=
ENST00000545985.5:c.1286A= (SLC37A4) ENSP00000475241.2:p.Glu429=
NM_001164277.1:c.1286A= , LRG_187t1:c.1286A= (SLC37A4) NP_001157749.1:p.Glu429=
NM_001164278.1:c.1352A= (SLC37A4) NP_001157750.1:p.Glu451=
NM_001164279.1:c.1067A= (SLC37A4) NP_001157751.1:p.Glu356=
NM_001164280.1:c.1286A= (SLC37A4) NP_001157752.1:p.Glu429=
NM_001467.5:c.1286A= (SLC37A4) NP_001458.1:p.Glu429=
NM_001164278.2:c.1352A= (SLC37A4) NP_001157750.1:p.Glu451=
NM_001164279.2:c.1067A= (SLC37A4) NP_001157751.1:p.Glu356=
NM_001164280.2:c.1286A= (SLC37A4) NP_001157752.1:p.Glu429=
NM_001467.6:c.1286A= (SLC37A4) NP_001458.1:p.Glu429=
NM_001164277.2:c.1286A= (SLC37A4) MANE Select NP_001157749.1:p.Glu429=