Canonical Allele Identifier: CA2003749722
Gene: SLC37A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119027760C= , CM000673.2:g.119027760C= GRCh38
NC_000011.9:g.118898470C= , CM000673.1:g.118898470C= GRCh37
NC_000011.8:g.118403680C= NCBI36
NG_013331.1:g.8147G= , LRG_187:g.8147G=

Transcript Alleles

HGVS Amino-acid change
ENST00000529510.6:n.723G=
ENST00000697845.1:n.647G=
ENST00000697846.1:n.723G=
ENST00000697847.1:n.723G=
ENST00000697848.1:n.723G=
ENST00000697849.1:n.1762G=
ENST00000697850.1:n.723G=
ENST00000697851.1:n.2083G=
ENST00000638186.1:n.797G=
ENST00000638360.1:n.629G=
ENST00000638925.1:n.730G=
ENST00000650539.1:n.899G=
ENST00000330775.9:c.494G= ENSP00000476242.2:p.Trp165=
ENST00000357590.9:c.494G= ENSP00000476176.2:p.Trp165=
ENST00000524428.5:n.815G=
ENST00000525039.5:n.917G=
ENST00000525102.5:n.1251G=
ENST00000525372.5:n.494G=
ENST00000526275.5:n.1275G=
ENST00000526626.6:n.456G=
ENST00000527992.5:n.721G=
ENST00000529510.5:n.399+434G=
ENST00000530407.5:n.643G=
ENST00000532085.1:n.3104G=
ENST00000532888.6:n.789G=
ENST00000538950.5:c.275G= ENSP00000475991.2:p.Trp92=
ENST00000545985.5:c.494G= ENSP00000475241.2:p.Trp165=
NM_001164277.1:c.494G= , LRG_187t1:c.494G= NP_001157749.1:p.Trp165=
NM_001164278.1:c.494G= NP_001157750.1:p.Trp165=
NM_001164279.1:c.275G= NP_001157751.1:p.Trp92=
NM_001164280.1:c.494G= NP_001157752.1:p.Trp165=
NM_001467.5:c.494G= NP_001458.1:p.Trp165=
NM_001164278.2:c.494G= NP_001157750.1:p.Trp165=
NM_001164279.2:c.275G= NP_001157751.1:p.Trp92=
NM_001164280.2:c.494G= NP_001157752.1:p.Trp165=
NM_001467.6:c.494G= NP_001458.1:p.Trp165=
NM_001164277.2:c.494G= MANE Select NP_001157749.1:p.Trp165=