Canonical Allele Identifier: CA912971035
Gene: SLC37A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119029292_119029296del , CM000673.2:g.119029292_119029296del GRCh38
NC_000011.9:g.118900002_118900006del , CM000673.1:g.118900002_118900006del GRCh37
NC_000011.8:g.118405212_118405216del NCBI36
NG_013331.1:g.6612_6616del , LRG_187:g.6612_6616del

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.304_308del
ENST00000697846.1:n.304_308del
ENST00000697847.1:n.304_308del
ENST00000697848.1:n.304_308del
ENST00000697849.1:n.548_552del
ENST00000697850.1:n.304_308del
ENST00000697851.1:n.548_552del
ENST00000638186.1:n.378_382del
ENST00000638360.1:n.312_316del
ENST00000638925.1:n.311_315del
ENST00000650539.1:n.480_484del
ENST00000330775.9:c.75_79del ENSP00000476242.2:p.Tyr25Ter
ENST00000357590.9:c.75_79del ENSP00000476176.2:p.Tyr25Ter
ENST00000524428.5:n.75_79del
ENST00000525039.5:n.498_502del
ENST00000525102.5:n.832_836del
ENST00000525372.5:n.75_79del
ENST00000525787.1:n.370_374del
ENST00000526626.6:n.270_274del
ENST00000527992.5:n.302_306del
ENST00000529510.5:n.93_97del
ENST00000530407.5:n.197+97_197+101del
ENST00000532085.1:n.1569_1573del
ENST00000532888.6:n.270_274del
ENST00000534384.1:n.295_299del
ENST00000538950.5:c.-172+97_-172+101del ENSP00000475991.2:n.-172+97_-172+101del
ENST00000545985.5:c.75_79del ENSP00000475241.2:p.Tyr25Ter
NM_001164277.1:c.75_79del , LRG_187t1:c.75_79del NP_001157749.1:p.Tyr25Ter
NM_001164278.1:c.75_79del NP_001157750.1:p.Tyr25Ter
NM_001164279.1:c.-172+97_-172+101del NP_001157751.1:n.-172+97_-172+101del
NM_001164280.1:c.75_79del NP_001157752.1:p.Tyr25Ter
NM_001467.5:c.75_79del NP_001458.1:p.Tyr25Ter
NM_001164278.2:c.75_79del NP_001157750.1:p.Tyr25Ter
NM_001164279.2:c.-172+97_-172+101del NP_001157751.1:n.-172+97_-172+101del
NM_001164280.2:c.75_79del NP_001157752.1:p.Tyr25Ter
NM_001467.6:c.75_79del NP_001458.1:p.Tyr25Ter
NM_001164277.2:c.75_79del MANE Select NP_001157749.1:p.Tyr25Ter