Canonical Allele Identifier: CA2003749697
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119027725_119027726delinsAC , CM000673.2:g.119027725_119027726delinsAC GRCh38
NC_000011.9:g.118898435_118898436delinsAC , CM000673.1:g.118898435_118898436delinsAC GRCh37
NC_000011.8:g.118403645_118403646delinsAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.757_758delinsGT
ENST00000697845.1:n.681_682delinsGT
ENST00000697846.1:n.757_758delinsGT
ENST00000697847.1:n.757_758delinsGT
ENST00000697848.1:n.757_758delinsGT
ENST00000697849.1:n.1796_1797delinsGT
ENST00000697850.1:n.757_758delinsGT
ENST00000697851.1:n.2117_2118delinsGT
ENST00000638186.1:n.831_832delinsGT
ENST00000638360.1:n.663_664delinsGT
ENST00000638925.1:n.764_765delinsGT
ENST00000650539.1:n.933_934delinsGT
ENST00000330775.9:c.528_529-1delinsGT
ENST00000357590.9:c.528_529-1delinsGT
ENST00000524428.5:n.849_850delinsGT
ENST00000525039.5:n.951_952delinsGT
ENST00000525102.5:n.1285_1286delinsGT
ENST00000525372.5:n.528_529delinsGT
ENST00000526275.5:n.1309_1310delinsGT
ENST00000526626.6:n.490_491delinsGT
ENST00000527992.5:n.755_756delinsGT
ENST00000529510.5:n.399+468_399+469delinsGT
ENST00000530407.5:n.677_678delinsGT
ENST00000532085.1:n.3138_3139delinsGT
ENST00000532888.6:n.823_824delinsGT
ENST00000538950.5:c.309_310-1delinsGT
ENST00000545985.5:c.528_529-1delinsGT