Canonical Allele Identifier: CA2616341115
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119029778_119029781del , CM000673.2:g.119029778_119029781del GRCh38
NC_000011.9:g.118900488_118900491del , CM000673.1:g.118900488_118900491del GRCh37
NC_000011.8:g.118405698_118405701del NCBI36
NG_013331.1:g.6126_6129del , LRG_187:g.6126_6129del

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.35-217_35-214del
ENST00000697846.1:n.35-217_35-214del
ENST00000697847.1:n.35-217_35-214del
ENST00000697848.1:n.35-217_35-214del
ENST00000697849.1:n.62_65del
ENST00000697850.1:n.35-217_35-214del
ENST00000697851.1:n.62_65del
ENST00000638186.1:n.108+86_108+89del
ENST00000638360.1:n.43-217_43-214del
ENST00000638925.1:n.42-217_42-214del
ENST00000650539.1:n.211-217_211-214del
ENST00000330775.9:c.-195-217_-195-214del ENSP00000476242.2:n.-195-217_-195-214del
ENST00000357590.9:c.-195-217_-195-214del ENSP00000476176.2:n.-195-217_-195-214del
ENST00000525039.5:n.229-217_229-214del
ENST00000525102.5:n.563-217_563-214del
ENST00000527992.5:n.33-217_33-214del
ENST00000530407.5:n.25-217_25-214del
ENST00000532085.1:n.1083_1086del
ENST00000534384.1:n.25+135_25+138del
ENST00000538950.5:c.-344-217_-344-214del ENSP00000475991.2:n.-344-217_-344-214del
ENST00000545985.5:c.-195-217_-195-214del ENSP00000475241.2:n.-195-217_-195-214del
NM_001164277.1:c.-195-217_-195-214del , LRG_187t1:c.-195-217_-195-214del NP_001157749.1:n.-195-217_-195-214del
NM_001164278.1:c.-195-217_-195-214del NP_001157750.1:n.-195-217_-195-214del
NM_001164279.1:c.-344-217_-344-214del NP_001157751.1:n.-344-217_-344-214del
NM_001467.5:c.-195-217_-195-214del NP_001458.1:n.-195-217_-195-214del
NM_001164278.2:c.-195-217_-195-214del NP_001157750.1:n.-195-217_-195-214del
NM_001164279.2:c.-344-217_-344-214del NP_001157751.1:n.-344-217_-344-214del
NM_001467.6:c.-195-217_-195-214del NP_001458.1:n.-195-217_-195-214del
NM_001164277.2:c.-195-217_-195-214del MANE Select NP_001157749.1:n.-195-217_-195-214del