Canonical Allele Identifier: CA2616341242
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119029939_119029946del , CM000673.2:g.119029939_119029946del GRCh38
NC_000011.9:g.118900649_118900656del , CM000673.1:g.118900649_118900656del GRCh37
NC_000011.8:g.118405859_118405866del NCBI36
NG_013331.1:g.5961_5968del , LRG_187:g.5961_5968del

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.35-382_35-375del
ENST00000697846.1:n.35-382_35-375del
ENST00000697847.1:n.35-382_35-375del
ENST00000697848.1:n.35-382_35-375del
ENST00000697850.1:n.35-382_35-375del
ENST00000638186.1:n.29_36del
ENST00000638360.1:n.43-382_43-375del
ENST00000638925.1:n.42-382_42-375del
ENST00000650539.1:n.210+224_210+231del
ENST00000330775.9:c.-195-382_-195-375del ENSP00000476242.2:n.-195-382_-195-375del
ENST00000357590.9:c.-195-382_-195-375del ENSP00000476176.2:n.-195-382_-195-375del
ENST00000525039.5:n.229-382_229-375del
ENST00000525102.5:n.562+286_562+293del
ENST00000527992.5:n.33-382_33-375del
ENST00000530407.5:n.25-382_25-375del
ENST00000532085.1:n.918_925del
ENST00000538950.5:c.-344-382_-344-375del ENSP00000475991.2:n.-344-382_-344-375del
ENST00000545985.5:c.-196+286_-196+293del ENSP00000475241.2:n.-196+286_-196+293del
NM_001164277.1:c.-196+286_-196+293del , LRG_187t1:c.-196+286_-196+293del NP_001157749.1:n.-196+286_-196+293del
NM_001164278.1:c.-195-382_-195-375del NP_001157750.1:n.-195-382_-195-375del
NM_001164279.1:c.-344-382_-344-375del NP_001157751.1:n.-344-382_-344-375del
NM_001467.5:c.-195-382_-195-375del NP_001458.1:n.-195-382_-195-375del
NM_001164278.2:c.-195-382_-195-375del NP_001157750.1:n.-195-382_-195-375del
NM_001164279.2:c.-344-382_-344-375del NP_001157751.1:n.-344-382_-344-375del
NM_001467.6:c.-195-382_-195-375del NP_001458.1:n.-195-382_-195-375del
NM_001164277.2:c.-196+286_-196+293del MANE Select NP_001157749.1:n.-196+286_-196+293del