Canonical Allele Identifier: CA2616341217
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119029920_119029922del , CM000673.2:g.119029920_119029922del GRCh38
NC_000011.9:g.118900630_118900632del , CM000673.1:g.118900630_118900632del GRCh37
NC_000011.8:g.118405840_118405842del NCBI36
NG_013331.1:g.5992_5994del , LRG_187:g.5992_5994del

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.35-351_35-349del
ENST00000697846.1:n.35-351_35-349del
ENST00000697847.1:n.35-351_35-349del
ENST00000697848.1:n.35-351_35-349del
ENST00000697850.1:n.35-351_35-349del
ENST00000638186.1:n.60_62del
ENST00000638360.1:n.43-351_43-349del
ENST00000638925.1:n.42-351_42-349del
ENST00000650539.1:n.210+255_210+257del
ENST00000330775.9:c.-195-351_-195-349del ENSP00000476242.2:n.-195-351_-195-349del
ENST00000357590.9:c.-195-351_-195-349del ENSP00000476176.2:n.-195-351_-195-349del
ENST00000525039.5:n.229-351_229-349del
ENST00000525102.5:n.562+317_562+319del
ENST00000527992.5:n.33-351_33-349del
ENST00000530407.5:n.25-351_25-349del
ENST00000532085.1:n.949_951del
ENST00000534384.1:n.25+1_25+3del
ENST00000538950.5:c.-344-351_-344-349del ENSP00000475991.2:n.-344-351_-344-349del
ENST00000545985.5:c.-196+317_-196+319del ENSP00000475241.2:n.-196+317_-196+319del
NM_001164277.1:c.-196+317_-196+319del , LRG_187t1:c.-196+317_-196+319del NP_001157749.1:n.-196+317_-196+319del
NM_001164278.1:c.-195-351_-195-349del NP_001157750.1:n.-195-351_-195-349del
NM_001164279.1:c.-344-351_-344-349del NP_001157751.1:n.-344-351_-344-349del
NM_001467.5:c.-195-351_-195-349del NP_001458.1:n.-195-351_-195-349del
NM_001164278.2:c.-195-351_-195-349del NP_001157750.1:n.-195-351_-195-349del
NM_001164279.2:c.-344-351_-344-349del NP_001157751.1:n.-344-351_-344-349del
NM_001467.6:c.-195-351_-195-349del NP_001458.1:n.-195-351_-195-349del
NM_001164277.2:c.-196+317_-196+319del MANE Select NP_001157749.1:n.-196+317_-196+319del