Canonical Allele Identifier: CA2003749940
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119028202G= , CM000673.2:g.119028202G= GRCh38
NC_000011.9:g.118898912G= , CM000673.1:g.118898912G= GRCh37
NC_000011.8:g.118404122G= NCBI36
NG_013331.1:g.7705C= , LRG_187:g.7705C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.602C=
ENST00000697845.1:n.526C=
ENST00000697846.1:n.602C=
ENST00000697847.1:n.602C=
ENST00000697848.1:n.602C=
ENST00000697849.1:n.1641C=
ENST00000697850.1:n.602C=
ENST00000697851.1:n.1641C=
ENST00000638186.1:n.676C=
ENST00000638360.1:n.610C=
ENST00000638925.1:n.609C=
ENST00000650539.1:n.778C=
ENST00000330775.9:c.373C= ENSP00000476242.2:p.Leu125=
ENST00000357590.9:c.373C= ENSP00000476176.2:p.Leu125=
ENST00000524428.5:n.373C=
ENST00000525039.5:n.796C=
ENST00000525102.5:n.1130C=
ENST00000525372.5:n.373C=
ENST00000525787.1:n.668C=
ENST00000526275.5:n.833C=
ENST00000526626.6:n.344-330C=
ENST00000527992.5:n.600C=
ENST00000529510.5:n.391C=
ENST00000530407.5:n.522C=
ENST00000532085.1:n.2662C=
ENST00000532888.6:n.668C=
ENST00000538950.5:c.154C= ENSP00000475991.2:p.Leu52=
ENST00000545985.5:c.373C= ENSP00000475241.2:p.Leu125=
NM_001164277.1:c.373C= , LRG_187t1:c.373C= NP_001157749.1:p.Leu125=
NM_001164278.1:c.373C= NP_001157750.1:p.Leu125=
NM_001164279.1:c.154C= NP_001157751.1:p.Leu52=
NM_001164280.1:c.373C= NP_001157752.1:p.Leu125=
NM_001467.5:c.373C= NP_001458.1:p.Leu125=
NM_001164278.2:c.373C= NP_001157750.1:p.Leu125=
NM_001164279.2:c.154C= NP_001157751.1:p.Leu52=
NM_001164280.2:c.373C= NP_001157752.1:p.Leu125=
NM_001467.6:c.373C= NP_001458.1:p.Leu125=
NM_001164277.2:c.373C= MANE Select NP_001157749.1:p.Leu125=