Canonical Allele Identifier: CA2695212790
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119027724del , CM000673.2:g.119027724del GRCh38
NC_000011.9:g.118898434del , CM000673.1:g.118898434del GRCh37
NC_000011.8:g.118403644del NCBI36
NG_013331.1:g.8182del , LRG_187:g.8182del

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.759del
ENST00000697845.1:n.683del
ENST00000697846.1:n.759del
ENST00000697847.1:n.759del
ENST00000697848.1:n.759del
ENST00000697849.1:n.1798del
ENST00000697850.1:n.759del
ENST00000697851.1:n.2119del
ENST00000638186.1:n.833del
ENST00000638360.1:n.665del
ENST00000638925.1:n.766del
ENST00000650539.1:n.935del
ENST00000330775.9:c.529del ENSP00000476242.2:p.Val177TrpfsTer?
ENST00000357590.9:c.529del ENSP00000476176.2:p.Val177TrpfsTer?
ENST00000524428.5:n.851del
ENST00000525039.5:n.953del
ENST00000525102.5:n.1287del
ENST00000525372.5:n.530del
ENST00000526275.5:n.1311del
ENST00000526626.6:n.492del
ENST00000527992.5:n.757del
ENST00000529510.5:n.399+470del
ENST00000530407.5:n.679del
ENST00000532085.1:n.3140del
ENST00000532888.6:n.825del
ENST00000538950.5:c.310del ENSP00000475991.2:p.Val104TrpfsTer?
ENST00000545985.5:c.529del ENSP00000475241.2:p.Val177TrpfsTer?
NM_001164277.1:c.529del , LRG_187t1:c.529del NP_001157749.1:p.Val177TrpfsTer?
NM_001164278.1:c.529del NP_001157750.1:p.Val177TrpfsTer?
NM_001164279.1:c.310del NP_001157751.1:p.Val104TrpfsTer?
NM_001164280.1:c.529del NP_001157752.1:p.Val177TrpfsTer?
NM_001467.5:c.529del NP_001458.1:p.Val177TrpfsTer?
NM_001164278.2:c.529del NP_001157750.1:p.Val177TrpfsTer?
NM_001164279.2:c.310del NP_001157751.1:p.Val104TrpfsTer?
NM_001164280.2:c.529del NP_001157752.1:p.Val177TrpfsTer?
NM_001467.6:c.529del NP_001458.1:p.Val177TrpfsTer?
NM_001164277.2:c.529del MANE Select NP_001157749.1:p.Val177TrpfsTer?