Canonical Allele Identifier: CA2003748325
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025074C= , CM000673.2:g.119025074C= GRCh38
NC_000011.9:g.118895784C= , CM000673.1:g.118895784C= GRCh37
NC_000011.8:g.118400994C= NCBI36
NG_013331.1:g.10832G= , LRG_187:g.10832G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1336G= (SLC37A4)
ENST00000697845.1:n.2325G= (SLC37A4)
ENST00000697846.1:n.1698G= (SLC37A4)
ENST00000697847.1:n.1409G= (SLC37A4)
ENST00000697849.1:n.3802G= (SLC37A4)
ENST00000697850.1:n.1993G= (SLC37A4)
ENST00000697851.1:n.2964G= (SLC37A4)
ENST00000638186.1:n.1430G= (SLC37A4)
ENST00000638360.1:n.1262G= (SLC37A4)
ENST00000638925.1:n.1395G= (SLC37A4)
ENST00000650539.1:n.1598G= (SLC37A4)
ENST00000330775.9:c.1126G= (SLC37A4) ENSP00000476242.2:p.Gly376=
ENST00000357590.9:c.1192G= (SLC37A4) ENSP00000476176.2:p.Gly398=
ENST00000524428.5:n.1362G= (SLC37A4)
ENST00000525039.5:n.1616G= (SLC37A4)
ENST00000525102.5:n.1884G= (SLC37A4)
ENST00000525372.5:n.1224G= (SLC37A4)
ENST00000526275.5:n.1908G= (SLC37A4)
ENST00000527992.5:n.1354G= (SLC37A4)
ENST00000530407.5:n.1276G= (SLC37A4)
ENST00000532085.1:n.5144G= (SLC37A4)
ENST00000533058.5:c.*25C= (TRAPPC4) ENSP00000432920.1:n.*25C=
ENST00000538950.5:c.907G= (SLC37A4) ENSP00000475991.2:p.Gly303=
ENST00000545985.5:c.1126G= (SLC37A4) ENSP00000475241.2:p.Gly376=
NM_001164277.1:c.1126G= , LRG_187t1:c.1126G= (SLC37A4) NP_001157749.1:p.Gly376=
NM_001164278.1:c.1192G= (SLC37A4) NP_001157750.1:p.Gly398=
NM_001164279.1:c.907G= (SLC37A4) NP_001157751.1:p.Gly303=
NM_001164280.1:c.1126G= (SLC37A4) NP_001157752.1:p.Gly376=
NM_001467.5:c.1126G= (SLC37A4) NP_001458.1:p.Gly376=
NM_001164278.2:c.1192G= (SLC37A4) NP_001157750.1:p.Gly398=
NM_001164279.2:c.907G= (SLC37A4) NP_001157751.1:p.Gly303=
NM_001164280.2:c.1126G= (SLC37A4) NP_001157752.1:p.Gly376=
NM_001467.6:c.1126G= (SLC37A4) NP_001458.1:p.Gly376=
NM_001164277.2:c.1126G= (SLC37A4) MANE Select NP_001157749.1:p.Gly376=