Canonical Allele Identifier: CA2616335830
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119027779_119027799del , CM000673.2:g.119027779_119027799del GRCh38
NC_000011.9:g.118898489_118898509del , CM000673.1:g.118898489_118898509del GRCh37
NC_000011.8:g.118403699_118403719del NCBI36
NG_013331.1:g.8108_8128del , LRG_187:g.8108_8128del

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.684_704del
ENST00000697845.1:n.608_628del
ENST00000697846.1:n.684_704del
ENST00000697847.1:n.684_704del
ENST00000697848.1:n.684_704del
ENST00000697849.1:n.1723_1743del
ENST00000697850.1:n.684_704del
ENST00000697851.1:n.2044_2064del
ENST00000638186.1:n.758_778del
ENST00000638360.1:n.619-29_619-9del
ENST00000638925.1:n.691_711del
ENST00000650539.1:n.860_880del
ENST00000330775.9:c.455_475del ENSP00000476242.2:p.Gly152_Leu159delinsVa...
ENST00000357590.9:c.455_475del ENSP00000476176.2:p.Gly152_Leu159delinsVa...
ENST00000524428.5:n.776_796del
ENST00000525039.5:n.878_898del
ENST00000525102.5:n.1212_1232del
ENST00000525372.5:n.455_475del
ENST00000526275.5:n.1236_1256del
ENST00000526626.6:n.417_437del
ENST00000527992.5:n.682_702del
ENST00000529510.5:n.399+395_399+415del
ENST00000530407.5:n.604_624del
ENST00000532085.1:n.3065_3085del
ENST00000532888.6:n.750_770del
ENST00000538950.5:c.236_256del ENSP00000475991.2:p.Gly79_Leu86delinsVal
ENST00000545985.5:c.455_475del ENSP00000475241.2:p.Gly152_Leu159delinsVa...
NM_001164277.1:c.455_475del , LRG_187t1:c.455_475del NP_001157749.1:p.Gly152_Leu159delinsVal
NM_001164278.1:c.455_475del NP_001157750.1:p.Gly152_Leu159delinsVal
NM_001164279.1:c.236_256del NP_001157751.1:p.Gly79_Leu86delinsVal
NM_001164280.1:c.455_475del NP_001157752.1:p.Gly152_Leu159delinsVal
NM_001467.5:c.455_475del NP_001458.1:p.Gly152_Leu159delinsVal
NM_001164278.2:c.455_475del NP_001157750.1:p.Gly152_Leu159delinsVal
NM_001164279.2:c.236_256del NP_001157751.1:p.Gly79_Leu86delinsVal
NM_001164280.2:c.455_475del NP_001157752.1:p.Gly152_Leu159delinsVal
NM_001467.6:c.455_475del NP_001458.1:p.Gly152_Leu159delinsVal
NM_001164277.2:c.455_475del MANE Select NP_001157749.1:p.Gly152_Leu159delinsVal