Canonical Allele Identifier: CA672397992
Gene: SLC37A4 HGNC NCBI

Linked Data

dbSNP Id: rs1288959953

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119030029_119030032del , CM000673.2:g.119030029_119030032del GRCh38
NC_000011.9:g.118900739_118900742del , CM000673.1:g.118900739_118900742del GRCh37
NC_000011.8:g.118405949_118405952del NCBI36
NG_013331.1:g.5877_5880del , LRG_187:g.5877_5880del

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.35-466_35-463del
ENST00000697846.1:n.35-466_35-463del
ENST00000697847.1:n.35-466_35-463del
ENST00000697848.1:n.35-466_35-463del
ENST00000697850.1:n.35-466_35-463del
ENST00000638360.1:n.43-466_43-463del
ENST00000638925.1:n.42-466_42-463del
ENST00000650539.1:n.210+140_210+143del
ENST00000330775.9:c.-195-466_-195-463del ENSP00000476242.2:n.-195-466_-195-463del
ENST00000357590.9:c.-195-466_-195-463del ENSP00000476176.2:n.-195-466_-195-463del
ENST00000525039.5:n.229-466_229-463del
ENST00000525102.5:n.562+202_562+205del
ENST00000527992.5:n.33-466_33-463del
ENST00000530407.5:n.25-466_25-463del
ENST00000532085.1:n.834_837del
ENST00000538950.5:c.-344-466_-344-463del ENSP00000475991.2:n.-344-466_-344-463del
ENST00000545985.5:c.-196+202_-196+205del ENSP00000475241.2:n.-196+202_-196+205del
NM_001164277.1:c.-196+202_-196+205del , LRG_187t1:c.-196+202_-196+205del NP_001157749.1:n.-196+202_-196+205del
NM_001164278.1:c.-195-466_-195-463del NP_001157750.1:n.-195-466_-195-463del
NM_001164279.1:c.-344-466_-344-463del NP_001157751.1:n.-344-466_-344-463del
NM_001467.5:c.-195-466_-195-463del NP_001458.1:n.-195-466_-195-463del
NM_001164278.2:c.-195-466_-195-463del NP_001157750.1:n.-195-466_-195-463del
NM_001164279.2:c.-344-466_-344-463del NP_001157751.1:n.-344-466_-344-463del
NM_001467.6:c.-195-466_-195-463del NP_001458.1:n.-195-466_-195-463del
NM_001164277.2:c.-196+202_-196+205del MANE Select NP_001157749.1:n.-196+202_-196+205del