Canonical Allele Identifier: CA2616340558
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119029090_119029093del , CM000673.2:g.119029090_119029093del GRCh38
NC_000011.9:g.118899800_118899803del , CM000673.1:g.118899800_118899803del GRCh37
NC_000011.8:g.118405010_118405013del NCBI36
NG_013331.1:g.6814_6817del , LRG_187:g.6814_6817del

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.377+129_377+132del
ENST00000697846.1:n.377+129_377+132del
ENST00000697847.1:n.377+129_377+132del
ENST00000697848.1:n.377+129_377+132del
ENST00000697849.1:n.750_753del
ENST00000697850.1:n.377+129_377+132del
ENST00000697851.1:n.750_753del
ENST00000638186.1:n.451+129_451+132del
ENST00000638360.1:n.385+129_385+132del
ENST00000638925.1:n.384+129_384+132del
ENST00000650539.1:n.553+129_553+132del
ENST00000330775.9:c.148+129_148+132del ENSP00000476242.2:n.148+129_148+132del
ENST00000357590.9:c.148+129_148+132del ENSP00000476176.2:n.148+129_148+132del
ENST00000524428.5:n.148+129_148+132del
ENST00000525039.5:n.571+129_571+132del
ENST00000525102.5:n.905+129_905+132del
ENST00000525372.5:n.148+129_148+132del
ENST00000525787.1:n.443+129_443+132del
ENST00000526626.6:n.343+129_343+132del
ENST00000527992.5:n.375+129_375+132del
ENST00000529510.5:n.166+129_166+132del
ENST00000530407.5:n.198-259_198-256del
ENST00000532085.1:n.1771_1774del
ENST00000532888.6:n.343+129_343+132del
ENST00000534384.1:n.368+129_368+132del
ENST00000538950.5:c.-171-259_-171-256del ENSP00000475991.2:n.-171-259_-171-256del
ENST00000545985.5:c.148+129_148+132del ENSP00000475241.2:n.148+129_148+132del
NM_001164277.1:c.148+129_148+132del , LRG_187t1:c.148+129_148+132del NP_001157749.1:n.148+129_148+132del
NM_001164278.1:c.148+129_148+132del NP_001157750.1:n.148+129_148+132del
NM_001164279.1:c.-171-259_-171-256del NP_001157751.1:n.-171-259_-171-256del
NM_001164280.1:c.148+129_148+132del NP_001157752.1:n.148+129_148+132del
NM_001467.5:c.148+129_148+132del NP_001458.1:n.148+129_148+132del
NM_001164278.2:c.148+129_148+132del NP_001157750.1:n.148+129_148+132del
NM_001164279.2:c.-171-259_-171-256del NP_001157751.1:n.-171-259_-171-256del
NM_001164280.2:c.148+129_148+132del NP_001157752.1:n.148+129_148+132del
NM_001467.6:c.148+129_148+132del NP_001458.1:n.148+129_148+132del
NM_001164277.2:c.148+129_148+132del MANE Select NP_001157749.1:n.148+129_148+132del