Canonical Allele Identifier: CA382896448
Gene: SLC37A4 HGNC NCBI
TRAPPC4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025326A>C , CM000673.2:g.119025326A>C GRCh38
NC_000011.9:g.118896036A>C , CM000673.1:g.118896036A>C GRCh37
NC_000011.8:g.118401246A>C NCBI36
NG_013331.1:g.10580T>G , LRG_187:g.10580T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000529510.6:n.1198T>G (SLC37A4)
ENST00000697845.1:n.2187T>G (SLC37A4)
ENST00000697846.1:n.1560T>G (SLC37A4)
ENST00000697847.1:n.1271T>G (SLC37A4)
ENST00000697849.1:n.3664T>G (SLC37A4)
ENST00000697850.1:n.1855T>G (SLC37A4)
ENST00000697851.1:n.2826T>G (SLC37A4)
ENST00000638186.1:n.1292T>G (SLC37A4)
ENST00000638360.1:n.1124T>G (SLC37A4)
ENST00000638925.1:n.1257T>G (SLC37A4)
ENST00000650539.1:n.1460T>G (SLC37A4)
ENST00000330775.9:c.988T>G (SLC37A4) ENSP00000476242.2:p.Trp330Gly
ENST00000357590.9:c.1054T>G (SLC37A4) ENSP00000476176.2:p.Trp352Gly
ENST00000524428.5:n.1224T>G (SLC37A4)
ENST00000525039.5:n.1478T>G (SLC37A4)
ENST00000525102.5:n.1746T>G (SLC37A4)
ENST00000525372.5:n.1086T>G (SLC37A4)
ENST00000526275.5:n.1770T>G (SLC37A4)
ENST00000527992.5:n.1216T>G (SLC37A4)
ENST00000529510.5:n.676T>G (SLC37A4)
ENST00000530407.5:n.1138T>G (SLC37A4)
ENST00000532085.1:n.5006T>G (SLC37A4)
ENST00000533058.5:c.*277A>C (TRAPPC4) ENSP00000432920.1:n.*277A>C
ENST00000538950.5:c.769T>G (SLC37A4) ENSP00000475991.2:p.Trp257Gly
ENST00000545985.5:c.988T>G (SLC37A4) ENSP00000475241.2:p.Trp330Gly
NM_001164277.1:c.988T>G , LRG_187t1:c.988T>G (SLC37A4) NP_001157749.1:p.Trp330Gly
NM_001164278.1:c.1054T>G (SLC37A4) NP_001157750.1:p.Trp352Gly
NM_001164279.1:c.769T>G (SLC37A4) NP_001157751.1:p.Trp257Gly
NM_001164280.1:c.988T>G (SLC37A4) NP_001157752.1:p.Trp330Gly
NM_001467.5:c.988T>G (SLC37A4) NP_001458.1:p.Trp330Gly
NM_001164278.2:c.1054T>G (SLC37A4) NP_001157750.1:p.Trp352Gly
NM_001164279.2:c.769T>G (SLC37A4) NP_001157751.1:p.Trp257Gly
NM_001164280.2:c.988T>G (SLC37A4) NP_001157752.1:p.Trp330Gly
NM_001467.6:c.988T>G (SLC37A4) NP_001458.1:p.Trp330Gly
NM_001164277.2:c.988T>G (SLC37A4) MANE Select NP_001157749.1:p.Trp330Gly