Canonical Allele Identifier: CA2003748236
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119024909_119024913delinsTTCAC , CM000673.2:g.119024909_119024913delinsTTCAC GRCh38
NC_000011.9:g.118895619_118895623delinsTTCAC , CM000673.1:g.118895619_118895623delinsTTCAC GRCh37
NC_000011.8:g.118400829_118400833delinsTTCAC NCBI36
NG_013331.1:g.10993_10997delinsGTGAA , LRG_187:g.10993_10997delinsGTGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1497_1501delinsGTGAA (SLC37A4)
ENST00000697845.1:n.2486_2490delinsGTGAA (SLC37A4)
ENST00000697846.1:n.1859_1863delinsGTGAA (SLC37A4)
ENST00000697847.1:n.1570_1574delinsGTGAA (SLC37A4)
ENST00000697849.1:n.3963_3967delinsGTGAA (SLC37A4)
ENST00000697850.1:n.2154_2158delinsGTGAA (SLC37A4)
ENST00000697851.1:n.3125_3129delinsGTGAA (SLC37A4)
ENST00000638186.1:n.1591_1595delinsGTGAA (SLC37A4)
ENST00000638360.1:n.1423_1427delinsGTGAA (SLC37A4)
ENST00000638925.1:n.1556_1560delinsGTGAA (SLC37A4)
ENST00000650539.1:n.1759_1763delinsGTGAA (SLC37A4)
ENST00000330775.9:c.1287_*1delinsGTGAA (SLC37A4) ENSP00000476242.2:n.[c.1287_*1delinsGTGAA;Glu429=]
ENST00000357590.9:c.1353_*1delinsGTGAA (SLC37A4) ENSP00000476176.2:n.[c.1353_*1delinsGTGAA;Glu451=]
ENST00000525102.5:n.2045_2049delinsGTGAA (SLC37A4)
ENST00000526275.5:n.2069_2073delinsGTGAA (SLC37A4)
ENST00000527992.5:n.1515_1519delinsGTGAA (SLC37A4)
ENST00000530407.5:n.1437_1441delinsGTGAA (SLC37A4)
ENST00000532085.1:n.5305_5309delinsGTGAA (SLC37A4)
ENST00000533058.5:c.634_638delinsTTCAC (TRAPPC4) ENSP00000432920.1:p.Phe212=
ENST00000538950.5:c.1068_*1delinsGTGAA (SLC37A4) ENSP00000475991.2:n.[c.1068_*1delinsGTGAA;Glu356=]
ENST00000545985.5:c.1287_*1delinsGTGAA (SLC37A4) ENSP00000475241.2:n.[c.1287_*1delinsGTGAA;Glu429=]
NM_001164277.1:c.1287_*1delinsGTGAA , LRG_187t1:c.1287_*1delinsGTGAA (SLC37A4) NP_001157749.1:n.[c.1287_*1delinsGTGAA;Glu429=]
NM_001164278.1:c.1353_*1delinsGTGAA (SLC37A4) NP_001157750.1:n.[c.1353_*1delinsGTGAA;Glu451=]
NM_001164279.1:c.1068_*1delinsGTGAA (SLC37A4) NP_001157751.1:n.[c.1068_*1delinsGTGAA;Glu356=]
NM_001164280.1:c.1287_*1delinsGTGAA (SLC37A4) NP_001157752.1:n.[c.1287_*1delinsGTGAA;Glu429=]
NM_001467.5:c.1287_*1delinsGTGAA (SLC37A4) NP_001458.1:n.[c.1287_*1delinsGTGAA;Glu429=]
NM_001164278.2:c.1353_*1delinsGTGAA (SLC37A4) NP_001157750.1:n.[c.1353_*1delinsGTGAA;Glu451=]
NM_001164279.2:c.1068_*1delinsGTGAA (SLC37A4) NP_001157751.1:n.[c.1068_*1delinsGTGAA;Glu356=]
NM_001164280.2:c.1287_*1delinsGTGAA (SLC37A4) NP_001157752.1:n.[c.1287_*1delinsGTGAA;Glu429=]
NM_001467.6:c.1287_*1delinsGTGAA (SLC37A4) NP_001458.1:n.[c.1287_*1delinsGTGAA;Glu429=]
NM_001164277.2:c.1287_*1delinsGTGAA (SLC37A4) MANE Select NP_001157749.1:n.[c.1287_*1delinsGTGAA;Glu429=]