Canonical Allele Identifier: CA2003749931
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119028188_119028193delinsACTCAC , CM000673.2:g.119028188_119028193delinsACTCAC GRCh38
NC_000011.9:g.118898898_118898903delinsACTCAC , CM000673.1:g.118898898_118898903delinsACTCAC GRCh37
NC_000011.8:g.118404108_118404113delinsACTCAC NCBI36
NG_013331.1:g.7714_7719delinsGTGAGT , LRG_187:g.7714_7719delinsGTGAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.610+1_610+6delinsGTGAGT
ENST00000697845.1:n.534+1_534+6delinsGTGAGT
ENST00000697846.1:n.610+1_610+6delinsGTGAGT
ENST00000697847.1:n.610+1_610+6delinsGTGAGT
ENST00000697848.1:n.610+1_610+6delinsGTGAGT
ENST00000697849.1:n.1649+1_1649+6delinsGTGAGT
ENST00000697850.1:n.610+1_610+6delinsGTGAGT
ENST00000697851.1:n.1650_1655delinsGTGAGT
ENST00000638186.1:n.684+1_684+6delinsGTGAGT
ENST00000638360.1:n.618+1_618+6delinsGTGAGT
ENST00000638925.1:n.617+1_617+6delinsGTGAGT
ENST00000650539.1:n.786+1_786+6delinsGTGAGT
ENST00000330775.9:c.381+1_381+6delinsGTGAGT ENSP00000476242.2:n.381+1_381+6delinsGTGAGT
ENST00000357590.9:c.381+1_381+6delinsGTGAGT ENSP00000476176.2:n.381+1_381+6delinsGTGAGT
ENST00000524428.5:n.382_387delinsGTGAGT
ENST00000525039.5:n.804+1_804+6delinsGTGAGT
ENST00000525102.5:n.1138+1_1138+6delinsGTGAGT
ENST00000525372.5:n.381+1_381+6delinsGTGAGT
ENST00000525787.1:n.677_682delinsGTGAGT
ENST00000526275.5:n.842_847delinsGTGAGT
ENST00000526626.6:n.344-321_344-316delinsGTGAGT
ENST00000527992.5:n.608+1_608+6delinsGTGAGT
ENST00000529510.5:n.399+1_399+6delinsGTGAGT
ENST00000530407.5:n.530+1_530+6delinsGTGAGT
ENST00000532085.1:n.2671_2676delinsGTGAGT
ENST00000532888.6:n.676+1_676+6delinsGTGAGT
ENST00000538950.5:c.162+1_162+6delinsGTGAGT ENSP00000475991.2:n.162+1_162+6delinsGTGAGT
ENST00000545985.5:c.381+1_381+6delinsGTGAGT ENSP00000475241.2:n.381+1_381+6delinsGTGAGT
NM_001164277.1:c.381+1_381+6delinsGTGAGT , LRG_187t1:c.381+1_381+6delinsGTGAGT NP_001157749.1:n.381+1_381+6delinsGTGAGT
NM_001164278.1:c.381+1_381+6delinsGTGAGT NP_001157750.1:n.381+1_381+6delinsGTGAGT
NM_001164279.1:c.162+1_162+6delinsGTGAGT NP_001157751.1:n.162+1_162+6delinsGTGAGT
NM_001164280.1:c.381+1_381+6delinsGTGAGT NP_001157752.1:n.381+1_381+6delinsGTGAGT
NM_001467.5:c.381+1_381+6delinsGTGAGT NP_001458.1:n.381+1_381+6delinsGTGAGT
NM_001164278.2:c.381+1_381+6delinsGTGAGT NP_001157750.1:n.381+1_381+6delinsGTGAGT
NM_001164279.2:c.162+1_162+6delinsGTGAGT NP_001157751.1:n.162+1_162+6delinsGTGAGT
NM_001164280.2:c.381+1_381+6delinsGTGAGT NP_001157752.1:n.381+1_381+6delinsGTGAGT
NM_001467.6:c.381+1_381+6delinsGTGAGT NP_001458.1:n.381+1_381+6delinsGTGAGT
NM_001164277.2:c.381+1_381+6delinsGTGAGT MANE Select NP_001157749.1:n.381+1_381+6delinsGTGAGT